Canonical Allele Identifier: CA1691303860
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298524G= , CM000669.2:g.17298524G= GRCh38
NC_000007.13:g.17338148G= , CM000669.1:g.17338148G= GRCh37
NC_000007.12:g.17304673G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1900G= ENSP00000495987.1:n.20+1900G=
XR_927069.1:n.13C=
XR_927070.1:n.13C=
XR_927071.1:n.13C=
XR_927072.1:n.14C=
XR_927073.1:n.15C=
XR_927073.2:n.15C=