Canonical Allele Identifier: CA1691255537
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244919C= , CM000669.2:g.17244919C= GRCh38
NC_000007.13:g.17284543C= , CM000669.1:g.17284543C= GRCh37
NC_000007.12:g.17251068C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2055C= ENSP00000495987.1:n.-955-2055C=
XR_927073.2:n.861+14333G=