Canonical Allele Identifier: CA836199948
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1003802683
gnomAD v3: 7-17293277-T-G
gnomAD v4: 7-17293277-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293277T>G , CM000669.2:g.17293277T>G GRCh38
NC_000007.13:g.17332901T>G , CM000669.1:g.17332901T>G GRCh37
NC_000007.12:g.17299426T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-3020T>G ENSP00000495987.1:n.-202-3020T>G
XR_927069.1:n.293+1889A>C
XR_927070.1:n.293+1889A>C
XR_927071.1:n.293+1889A>C
XR_927072.1:n.294+1889A>C
XR_927073.1:n.295+1889A>C
XR_927073.2:n.295+1889A>C