Canonical Allele Identifier: CA573132049

Gene: AHR

Linked Data

• dbSNP Id: rs1412037768
• gnomAD v2: 7-17333050-A-G
• gnomAD v3: 7-17293426-A-G
• gnomAD v4: 7-17293426-A-G
• MyVariant Identifiers: chr7:g.17333050A>G (hg19) ; chr7:g.17293426A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293426A>G , CM000669.2:g.17293426A>G	GRCh38
NC_000007.13:g.17333050A>G , CM000669.1:g.17333050A>G	GRCh37
NC_000007.12:g.17299575A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-2871A>G	ENSP00000495987.1:n.-202-2871A>G
XR_927069.1:n.293+1740T>C
XR_927070.1:n.293+1740T>C
XR_927071.1:n.293+1740T>C
XR_927072.1:n.294+1740T>C
XR_927073.1:n.295+1740T>C
XR_927073.2:n.295+1740T>C