Canonical Allele Identifier: CA154826870
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs368990710
gnomAD v3: 7-17285593-T-C
gnomAD v4: 7-17285593-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285593T>C , CM000669.2:g.17285593T>C GRCh38
NC_000007.13:g.17325217T>C , CM000669.1:g.17325217T>C GRCh37
NC_000007.12:g.17291742T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10704T>C ENSP00000495987.1:n.-202-10704T>C
XR_927069.1:n.567+650A>G
XR_927070.1:n.567+650A>G
XR_927071.1:n.567+650A>G
XR_927072.1:n.568+650A>G
XR_927073.2:n.711+650A>G