Canonical Allele Identifier: CA836200081
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1268575521

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293397_17293398insT , CM000669.2:g.17293397_17293398insT GRCh38
NC_000007.13:g.17333021_17333022insT , CM000669.1:g.17333021_17333022insT GRCh37
NC_000007.12:g.17299546_17299547insT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2900_-202-2899insT ENSP00000495987.1:n.-202-2900_-202-2899in...
XR_927069.1:n.293+1768_293+1769insA
XR_927070.1:n.293+1768_293+1769insA
XR_927071.1:n.293+1768_293+1769insA
XR_927072.1:n.294+1768_294+1769insA
XR_927073.1:n.295+1768_295+1769insA
XR_927073.2:n.295+1768_295+1769insA