Canonical Allele Identifier: CA1098896383
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293303_17293304insTTTT , CM000669.2:g.17293303_17293304insTTTT GRCh38
NC_000007.13:g.17332927_17332928insTTTT , CM000669.1:g.17332927_17332928insTTTT GRCh37
NC_000007.12:g.17299452_17299453insTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2994_-202-2993insTTTT ENSP00000495987.1:n.-202-2994_-202-2993insTTTT
XR_927069.1:n.293+1863_293+1864insAAAA
XR_927070.1:n.293+1863_293+1864insAAAA
XR_927071.1:n.293+1863_293+1864insAAAA
XR_927072.1:n.294+1863_294+1864insAAAA
XR_927073.1:n.295+1863_295+1864insAAAA
XR_927073.2:n.295+1863_295+1864insAAAA