Canonical Allele Identifier: CA836200043
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1160955898

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293352_17293358del , CM000669.2:g.17293352_17293358del GRCh38
NC_000007.13:g.17332976_17332982del , CM000669.1:g.17332976_17332982del GRCh37
NC_000007.12:g.17299501_17299507del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2945_-202-2939del ENSP00000495987.1:n.-202-2945_-202-2939de...
XR_927069.1:n.293+1811_293+1817del
XR_927070.1:n.293+1811_293+1817del
XR_927071.1:n.293+1811_293+1817del
XR_927072.1:n.294+1811_294+1817del
XR_927073.1:n.295+1811_295+1817del
XR_927073.2:n.295+1811_295+1817del