Canonical Allele Identifier: CA154826864
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs889977416

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285550_17285551del , CM000669.2:g.17285550_17285551del GRCh38
NC_000007.13:g.17325174_17325175del , CM000669.1:g.17325174_17325175del GRCh37
NC_000007.12:g.17291699_17291700del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10747_-202-10746del ENSP00000495987.1:n.-202-10747_-202-10746...
XR_927069.1:n.567+695_567+696del
XR_927070.1:n.567+695_567+696del
XR_927071.1:n.567+695_567+696del
XR_927072.1:n.568+695_568+696del
XR_927073.2:n.711+695_711+696del