Canonical Allele Identifier: CA1691258342
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247567C= , CM000669.2:g.17247567C= GRCh38
NC_000007.13:g.17287191C= , CM000669.1:g.17287191C= GRCh37
NC_000007.12:g.17253716C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-362C= ENSP00000495987.1:n.-362C=
XR_927073.2:n.861+11685G=