Canonical Allele Identifier: CA1691290777
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269557T= , CM000669.2:g.17269557T= GRCh38
NC_000007.13:g.17309181T= , CM000669.1:g.17309181T= GRCh37
NC_000007.12:g.17275706T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-203+21831T= ENSP00000495987.1:n.-203+21831T=
XR_927073.2:n.785-10229A=