Canonical Allele Identifier: CA1691303908
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298541G= , CM000669.2:g.17298541G= GRCh38
NC_000007.13:g.17338165G= , CM000669.1:g.17338165G= GRCh37
NC_000007.12:g.17304690G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.20+1917G= ENSP00000495987.1:n.20+1917G=