Canonical Allele Identifier: CA1691255542
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244929A= , CM000669.2:g.17244929A= GRCh38
NC_000007.13:g.17284553A= , CM000669.1:g.17284553A= GRCh37
NC_000007.12:g.17251078A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2045A= ENSP00000495987.1:n.-955-2045A=
XR_927073.2:n.861+14323T=