ClinVar

NM_003977.4(AIP):c.645+7C>T

Gene:

AIP:aryl hydrocarbon receptor interacting protein [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.2

Genomic location:

• Chr11: 67490221 (on Assembly GRCh38)
• Chr11: 67257692 (on Assembly GRCh37)

Preferred name:

NM_003977.4(AIP):c.645+7C>T

HGVS:

• NC_000011.10:g.67490221C>T
• NG_008969.1:g.12188C>T
• NM_001302959.2:c.468+7C>T
• NM_001302960.2:c.645+7C>T
• NM_003977.4:c.645+7C>TMANE SELECT
• LRG_460:g.12188C>T
• NC_000011.9:g.67257692C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001302959.2:c.468+7C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001302960.2:c.645+7C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_003977.4:c.645+7C>T - intron variant - [Sequence Ontology: SO:0001627]