Canonical Allele Identifier: CA1098896503
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781838288
gnomAD v3: 7-17293475-A-G
gnomAD v4: 7-17293475-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293475A>G , CM000669.2:g.17293475A>G GRCh38
NC_000007.13:g.17333099A>G , CM000669.1:g.17333099A>G GRCh37
NC_000007.12:g.17299624A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2822A>G ENSP00000495987.1:n.-202-2822A>G
XR_927069.1:n.293+1691T>C
XR_927070.1:n.293+1691T>C
XR_927071.1:n.293+1691T>C
XR_927072.1:n.294+1691T>C
XR_927073.1:n.295+1691T>C
XR_927073.2:n.295+1691T>C