Canonical Allele Identifier: CA1691298702
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293183G= , CM000669.2:g.17293183G= GRCh38
NC_000007.13:g.17332807G= , CM000669.1:g.17332807G= GRCh37
NC_000007.12:g.17299332G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-3114G= ENSP00000495987.1:n.-202-3114G=
XR_927069.1:n.293+1983C=
XR_927070.1:n.293+1983C=
XR_927071.1:n.293+1983C=
XR_927072.1:n.294+1983C=
XR_927073.1:n.296-1812C=
XR_927073.2:n.296-1812C=