Canonical Allele Identifier: CA1691298930
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs552926271

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293427C>A , CM000669.2:g.17293427C>A GRCh38
NC_000007.13:g.17333051C>A , CM000669.1:g.17333051C>A GRCh37
NC_000007.12:g.17299576C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2870C>A ENSP00000495987.1:n.-202-2870C>A
XR_927069.1:n.293+1739G>T
XR_927070.1:n.293+1739G>T
XR_927071.1:n.293+1739G>T
XR_927072.1:n.294+1739G>T
XR_927073.1:n.295+1739G>T
XR_927073.2:n.295+1739G>T