Canonical Allele Identifier: CA2774555321
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293302C>A , CM000669.2:g.17293302C>A GRCh38
NC_000007.13:g.17332926C>A , CM000669.1:g.17332926C>A GRCh37
NC_000007.12:g.17299451C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2995C>A ENSP00000495987.1:n.-202-2995C>A
XR_927069.1:n.293+1864G>T
XR_927070.1:n.293+1864G>T
XR_927071.1:n.293+1864G>T
XR_927072.1:n.294+1864G>T
XR_927073.1:n.295+1864G>T
XR_927073.2:n.295+1864G>T