Canonical Allele Identifier: CA1691255534
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244904T= , CM000669.2:g.17244904T= GRCh38
NC_000007.13:g.17284528T= , CM000669.1:g.17284528T= GRCh37
NC_000007.12:g.17251053T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2070T= ENSP00000495987.1:n.-955-2070T=
XR_927073.2:n.861+14348A=