Canonical Allele Identifier: CA1691298750
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1584023053

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293259T>G , CM000669.2:g.17293259T>G GRCh38
NC_000007.13:g.17332883T>G , CM000669.1:g.17332883T>G GRCh37
NC_000007.12:g.17299408T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-3038T>G ENSP00000495987.1:n.-202-3038T>G
XR_927069.1:n.293+1907A>C
XR_927070.1:n.293+1907A>C
XR_927071.1:n.293+1907A>C
XR_927072.1:n.294+1907A>C
XR_927073.1:n.296-1888A>C
XR_927073.2:n.296-1888A>C