Canonical Allele Identifier: CA1691298998
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293507A= , CM000669.2:g.17293507A= GRCh38
NC_000007.13:g.17333131A= , CM000669.1:g.17333131A= GRCh37
NC_000007.12:g.17299656A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2790A= ENSP00000495987.1:n.-202-2790A=
XR_927069.1:n.293+1659T=
XR_927070.1:n.293+1659T=
XR_927071.1:n.293+1659T=
XR_927072.1:n.294+1659T=
XR_927073.1:n.295+1659T=
XR_927073.2:n.295+1659T=