Canonical Allele Identifier: CA12458237
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs6968865
gnomAD v2: 7-17287269-A-T
gnomAD v3: 7-17247645-A-T
gnomAD v4: 7-17247645-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247645A>T , CM000669.2:g.17247645A>T GRCh38
NC_000007.13:g.17287269A>T , CM000669.1:g.17287269A>T GRCh37
NC_000007.12:g.17253794A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-284A>T ENSP00000495987.1:n.-284A>T
XR_927073.2:n.861+11607T>A