Canonical Allele Identifier: CA836195659

Gene: AHR

Linked Data

• dbSNP Id: rs1425012290
• gnomAD v3: 7-17285397-T-C
• gnomAD v4: 7-17285397-T-C
• MyVariant Identifiers: chr7:g.17325021T>C (hg19) ; chr7:g.17285397T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285397T>C , CM000669.2:g.17285397T>C	GRCh38
NC_000007.13:g.17325021T>C , CM000669.1:g.17325021T>C	GRCh37
NC_000007.12:g.17291546T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-10900T>C	ENSP00000495987.1:n.-202-10900T>C
XR_927069.1:n.567+846A>G
XR_927070.1:n.567+846A>G
XR_927071.1:n.567+846A>G
XR_927072.1:n.568+846A>G
XR_927073.2:n.711+846A>G