Canonical Allele Identifier: CA1691291824

Gene: AHR

Linked Data

• dbSNP Id: rs1584020006

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285542G>A , CM000669.2:g.17285542G>A	GRCh38
NC_000007.13:g.17325166G>A , CM000669.1:g.17325166G>A	GRCh37
NC_000007.12:g.17291691G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-10755G>A	ENSP00000495987.1:n.-202-10755G>A
XR_927069.1:n.567+701C>T
XR_927070.1:n.567+701C>T
XR_927071.1:n.567+701C>T
XR_927072.1:n.568+701C>T
XR_927073.2:n.711+701C>T