Canonical Allele Identifier: CA1691303912

Gene: AHR

Linked Data

• dbSNP Id: rs1329077659
• gnomAD v4: 7-17298543-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17298543C>T , CM000669.2:g.17298543C>T	GRCh38
NC_000007.13:g.17338167C>T , CM000669.1:g.17338167C>T	GRCh37
NC_000007.12:g.17304692C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.20+1919C>T	ENSP00000495987.1:n.20+1919C>T