Canonical Allele Identifier: CA154828312
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs984990871
gnomAD v2: 7-17338054-T-C
gnomAD v3: 7-17298430-T-C
gnomAD v4: 7-17298430-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298430T>C , CM000669.2:g.17298430T>C GRCh38
NC_000007.13:g.17338054T>C , CM000669.1:g.17338054T>C GRCh37
NC_000007.12:g.17304579T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.20+1806T>C ENSP00000495987.1:n.20+1806T>C
XR_927069.1:n.107A>G
XR_927070.1:n.107A>G
XR_927071.1:n.107A>G
XR_927072.1:n.108A>G
XR_927073.1:n.109A>G
XR_927073.2:n.109A>G