Canonical Allele Identifier: CA1691303883
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781909963
gnomAD v4: 7-17298532-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298532A>C , CM000669.2:g.17298532A>C GRCh38
NC_000007.13:g.17338156A>C , CM000669.1:g.17338156A>C GRCh37
NC_000007.12:g.17304681A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1908A>C ENSP00000495987.1:n.20+1908A>C
XR_927069.1:n.5T>G
XR_927070.1:n.5T>G
XR_927071.1:n.5T>G
XR_927072.1:n.6T>G
XR_927073.1:n.7T>G
XR_927073.2:n.7T>G