Canonical Allele Identifier: CA1691298779
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293286G= , CM000669.2:g.17293286G= GRCh38
NC_000007.13:g.17332910G= , CM000669.1:g.17332910G= GRCh37
NC_000007.12:g.17299435G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-3011G= ENSP00000495987.1:n.-202-3011G=
XR_927069.1:n.293+1880C=
XR_927070.1:n.293+1880C=
XR_927071.1:n.293+1880C=
XR_927072.1:n.294+1880C=
XR_927073.1:n.295+1880C=
XR_927073.2:n.295+1880C=