Canonical Allele Identifier: CA836203378
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1254394346
gnomAD v3: 7-17298538-A-T
gnomAD v4: 7-17298538-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298538A>T , CM000669.2:g.17298538A>T GRCh38
NC_000007.13:g.17338162A>T , CM000669.1:g.17338162A>T GRCh37
NC_000007.12:g.17304687A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1914A>T ENSP00000495987.1:n.20+1914A>T
XR_927073.1:n.1T>A
XR_927073.2:n.1T>A