ClinVar

NM_005184.4(CALM3):c.179-13C>T

Gene:

CALM3:calmodulin 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.32

Genomic location:

• Chr19: 46608469 (on Assembly GRCh38)
• Chr19: 47111726 (on Assembly GRCh37)

Preferred name:

NM_005184.4(CALM3):c.179-13C>T

HGVS:

• NC_000019.10:g.46608469C>T
• NG_051331.1:g.12396C>T
• NM_001329921.1:c.71-13C>T
• NM_001329922.1:c.179-13C>T
• NM_001329923.1:c.71-13C>T
• NM_001329924.2:c.71-13C>T
• NM_001329925.2:c.71-13C>T
• NM_001329926.2:c.71-13C>T
• NM_005184.4:c.179-13C>TMANE SELECT
• LRG_1082t1:c.179-13C>T
• LRG_1082:g.12396C>T
• NC_000019.9:g.47111726C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001329921.1:c.71-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001329922.1:c.179-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001329923.1:c.71-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001329924.2:c.71-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001329925.2:c.71-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001329926.2:c.71-13C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_005184.4:c.179-13C>T - intron variant - [Sequence Ontology: SO:0001627]