Canonical Allele Identifier: CA1691298670
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293146G= , CM000669.2:g.17293146G= GRCh38
NC_000007.13:g.17332770G= , CM000669.1:g.17332770G= GRCh37
NC_000007.12:g.17299295G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-3151G= ENSP00000495987.1:n.-202-3151G=
XR_927069.1:n.293+2020C=
XR_927070.1:n.293+2020C=
XR_927071.1:n.293+2020C=
XR_927072.1:n.294+2020C=
XR_927073.1:n.296-1775C=
XR_927073.2:n.296-1775C=