Canonical Allele Identifier: CA1691299031
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781842445

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293561T>C , CM000669.2:g.17293561T>C GRCh38
NC_000007.13:g.17333185T>C , CM000669.1:g.17333185T>C GRCh37
NC_000007.12:g.17299710T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2736T>C ENSP00000495987.1:n.-202-2736T>C
XR_927069.1:n.293+1605A>G
XR_927070.1:n.293+1605A>G
XR_927071.1:n.293+1605A>G
XR_927072.1:n.294+1605A>G
XR_927073.1:n.295+1605A>G
XR_927073.2:n.295+1605A>G