Canonical Allele Identifier: CA1691298725
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293221C= , CM000669.2:g.17293221C= GRCh38
NC_000007.13:g.17332845C= , CM000669.1:g.17332845C= GRCh37
NC_000007.12:g.17299370C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-3076C= ENSP00000495987.1:n.-202-3076C=
XR_927069.1:n.293+1945G=
XR_927070.1:n.293+1945G=
XR_927071.1:n.293+1945G=
XR_927072.1:n.294+1945G=
XR_927073.1:n.296-1850G=
XR_927073.2:n.296-1850G=