Canonical Allele Identifier: CA1691303618
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298427G= , CM000669.2:g.17298427G= GRCh38
NC_000007.13:g.17338051G= , CM000669.1:g.17338051G= GRCh37
NC_000007.12:g.17304576G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1803G= ENSP00000495987.1:n.20+1803G=
XR_927069.1:n.110C=
XR_927070.1:n.110C=
XR_927071.1:n.110C=
XR_927072.1:n.111C=
XR_927073.1:n.112C=
XR_927073.2:n.112C=