Canonical Allele Identifier: CA836203386

Gene: AHR

Linked Data

• dbSNP Id: rs1265527671
• gnomAD v3: 7-17298541-G-A
• gnomAD v4: 7-17298541-G-A
• MyVariant Identifiers: chr7:g.17338165G>A (hg19) ; chr7:g.17298541G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17298541G>A , CM000669.2:g.17298541G>A	GRCh38
NC_000007.13:g.17338165G>A , CM000669.1:g.17338165G>A	GRCh37
NC_000007.12:g.17304690G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.20+1917G>A	ENSP00000495987.1:n.20+1917G>A