Canonical Allele Identifier: CA1691298633
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293105C= , CM000669.2:g.17293105C= GRCh38
NC_000007.13:g.17332729C= , CM000669.1:g.17332729C= GRCh37
NC_000007.12:g.17299254C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-3192C= ENSP00000495987.1:n.-202-3192C=
XR_927069.1:n.293+2061G=
XR_927070.1:n.293+2061G=
XR_927071.1:n.293+2061G=
XR_927072.1:n.294+2061G=
XR_927073.1:n.296-1734G=
XR_927073.2:n.296-1734G=