Canonical Allele Identifier: CA1691298753

Gene: AHR

Linked Data

• dbSNP Id: rs1403654104

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293262C>T , CM000669.2:g.17293262C>T	GRCh38
NC_000007.13:g.17332886C>T , CM000669.1:g.17332886C>T	GRCh37
NC_000007.12:g.17299411C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-3035C>T	ENSP00000495987.1:n.-202-3035C>T
XR_927069.1:n.293+1904G>A
XR_927070.1:n.293+1904G>A
XR_927071.1:n.293+1904G>A
XR_927072.1:n.294+1904G>A
XR_927073.1:n.296-1891G>A
XR_927073.2:n.296-1891G>A