Canonical Allele Identifier: CA836203385

Gene: AHR

Linked Data

• dbSNP Id: rs1461881829
• gnomAD v3: 7-17298540-G-A
• gnomAD v4: 7-17298540-G-A
• MyVariant Identifiers: chr7:g.17338164G>A (hg19) ; chr7:g.17298540G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17298540G>A , CM000669.2:g.17298540G>A	GRCh38
NC_000007.13:g.17338164G>A , CM000669.1:g.17338164G>A	GRCh37
NC_000007.12:g.17304689G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.20+1916G>A	ENSP00000495987.1:n.20+1916G>A