Canonical Allele Identifier: CA1691291707
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781752161

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285400A>G , CM000669.2:g.17285400A>G GRCh38
NC_000007.13:g.17325024A>G , CM000669.1:g.17325024A>G GRCh37
NC_000007.12:g.17291549A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10897A>G ENSP00000495987.1:n.-202-10897A>G
XR_927069.1:n.567+843T>C
XR_927070.1:n.567+843T>C
XR_927071.1:n.567+843T>C
XR_927072.1:n.568+843T>C
XR_927073.2:n.711+843T>C