ClinVar

NM_001164277.2(SLC37A4):c.872-4A>G

Gene:

SLC37A4:solute carrier family 37 member 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.3

Genomic location:

• Chr11: 119026084 (on Assembly GRCh38)
• Chr11: 118896794 (on Assembly GRCh37)

Preferred name:

NM_001164277.2(SLC37A4):c.872-4A>G

HGVS:

• NC_000011.10:g.119026084T>C
• NG_013331.1:g.9822A>G
• NM_001164277.2:c.872-4A>GMANE SELECT
• NM_001164278.2:c.872-4A>G
• NM_001164279.2:c.653-4A>G
• NM_001164280.2:c.872-4A>G
• NM_001467.6:c.872-4A>G
• LRG_187:g.9822A>G
• NC_000011.9:g.118896794T>C

This HGVS expression did not pass validation

Molecular consequence:

• NM_001164277.2:c.872-4A>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001164278.2:c.872-4A>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001164279.2:c.653-4A>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001164280.2:c.872-4A>G - intron variant - [Sequence Ontology: SO:0001627]
• NM_001467.6:c.872-4A>G - intron variant - [Sequence Ontology: SO:0001627]