Canonical Allele Identifier: CA154826872
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs571371013
gnomAD v2: 7-17325234-C-A
gnomAD v3: 7-17285610-C-A
gnomAD v4: 7-17285610-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285610C>A , CM000669.2:g.17285610C>A GRCh38
NC_000007.13:g.17325234C>A , CM000669.1:g.17325234C>A GRCh37
NC_000007.12:g.17291759C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10687C>A ENSP00000495987.1:n.-202-10687C>A
XR_927069.1:n.567+633G>T
XR_927070.1:n.567+633G>T
XR_927071.1:n.567+633G>T
XR_927072.1:n.568+633G>T
XR_927073.2:n.711+633G>T