Canonical Allele Identifier: CA836200059
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1286194690

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293374_17293377del , CM000669.2:g.17293374_17293377del GRCh38
NC_000007.13:g.17332998_17333001del , CM000669.1:g.17332998_17333001del GRCh37
NC_000007.12:g.17299523_17299526del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2923_-202-2920del ENSP00000495987.1:n.-202-2923_-202-2920de...
XR_927069.1:n.293+1792_293+1795del
XR_927070.1:n.293+1792_293+1795del
XR_927071.1:n.293+1792_293+1795del
XR_927072.1:n.294+1792_294+1795del
XR_927073.1:n.295+1792_295+1795del
XR_927073.2:n.295+1792_295+1795del