Canonical Allele Identifier: CA836203387

Gene: AHR

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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