Canonical Allele Identifier: CA1691298844
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293365C= , CM000669.2:g.17293365C= GRCh38
NC_000007.13:g.17332989C= , CM000669.1:g.17332989C= GRCh37
NC_000007.12:g.17299514C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2932C= ENSP00000495987.1:n.-202-2932C=
XR_927069.1:n.293+1801G=
XR_927070.1:n.293+1801G=
XR_927071.1:n.293+1801G=
XR_927072.1:n.294+1801G=
XR_927073.1:n.295+1801G=
XR_927073.2:n.295+1801G=