Canonical Allele Identifier: CA154827761
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs909960536
gnomAD v2: 7-17333096-A-G
gnomAD v3: 7-17293472-A-G
gnomAD v4: 7-17293472-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293472A>G , CM000669.2:g.17293472A>G GRCh38
NC_000007.13:g.17333096A>G , CM000669.1:g.17333096A>G GRCh37
NC_000007.12:g.17299621A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2825A>G ENSP00000495987.1:n.-202-2825A>G
XR_927069.1:n.293+1694T>C
XR_927070.1:n.293+1694T>C
XR_927071.1:n.293+1694T>C
XR_927072.1:n.294+1694T>C
XR_927073.1:n.295+1694T>C
XR_927073.2:n.295+1694T>C