Canonical Allele Identifier: CA154826873
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs537116348
gnomAD v2: 7-17325236-A-C
gnomAD v3: 7-17285612-A-C
gnomAD v4: 7-17285612-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285612A>C , CM000669.2:g.17285612A>C GRCh38
NC_000007.13:g.17325236A>C , CM000669.1:g.17325236A>C GRCh37
NC_000007.12:g.17291761A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10685A>C ENSP00000495987.1:n.-202-10685A>C
XR_927069.1:n.567+631T>G
XR_927070.1:n.567+631T>G
XR_927071.1:n.567+631T>G
XR_927072.1:n.568+631T>G
XR_927073.2:n.711+631T>G