Canonical Allele Identifier: CA1691303873
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298527A= , CM000669.2:g.17298527A= GRCh38
NC_000007.13:g.17338151A= , CM000669.1:g.17338151A= GRCh37
NC_000007.12:g.17304676A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1903A= ENSP00000495987.1:n.20+1903A=
XR_927069.1:n.10T=
XR_927070.1:n.10T=
XR_927071.1:n.10T=
XR_927072.1:n.11T=
XR_927073.1:n.12T=
XR_927073.2:n.12T=