Canonical Allele Identifier: CA1691303634
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298435A= , CM000669.2:g.17298435A= GRCh38
NC_000007.13:g.17338059A= , CM000669.1:g.17338059A= GRCh37
NC_000007.12:g.17304584A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1811A= ENSP00000495987.1:n.20+1811A=
XR_927069.1:n.102T=
XR_927070.1:n.102T=
XR_927071.1:n.102T=
XR_927072.1:n.103T=
XR_927073.1:n.104T=
XR_927073.2:n.104T=