Canonical Allele Identifier: CA1691298741
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs964519142

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293236G>A , CM000669.2:g.17293236G>A GRCh38
NC_000007.13:g.17332860G>A , CM000669.1:g.17332860G>A GRCh37
NC_000007.12:g.17299385G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-3061G>A ENSP00000495987.1:n.-202-3061G>A
XR_927069.1:n.293+1930C>T
XR_927070.1:n.293+1930C>T
XR_927071.1:n.293+1930C>T
XR_927072.1:n.294+1930C>T
XR_927073.1:n.296-1865C>T
XR_927073.2:n.296-1865C>T