Canonical Allele Identifier: CA1691290779
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269561T= , CM000669.2:g.17269561T= GRCh38
NC_000007.13:g.17309185T= , CM000669.1:g.17309185T= GRCh37
NC_000007.12:g.17275710T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-203+21835T= ENSP00000495987.1:n.-203+21835T=
XR_927073.2:n.785-10233A=