Canonical Allele Identifier: CA836199982
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1202633931

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293284_17293285del , CM000669.2:g.17293284_17293285del GRCh38
NC_000007.13:g.17332908_17332909del , CM000669.1:g.17332908_17332909del GRCh37
NC_000007.12:g.17299433_17299434del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-3013_-202-3012del ENSP00000495987.1:n.-202-3013_-202-3012de...
XR_927069.1:n.293+1881_293+1882del
XR_927070.1:n.293+1881_293+1882del
XR_927071.1:n.293+1881_293+1882del
XR_927072.1:n.294+1881_294+1882del
XR_927073.1:n.295+1881_295+1882del
XR_927073.2:n.295+1881_295+1882del