Canonical Allele Identifier: CA1691290811
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781588789

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269588A>G , CM000669.2:g.17269588A>G GRCh38
NC_000007.13:g.17309212A>G , CM000669.1:g.17309212A>G GRCh37
NC_000007.12:g.17275737A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-203+21862A>G ENSP00000495987.1:n.-203+21862A>G
XR_927073.2:n.785-10260T>C