Canonical Allele Identifier: CA1691298773
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293283_17293285delinsCCA , CM000669.2:g.17293283_17293285delinsCCA GRCh38
NC_000007.13:g.17332907_17332909delinsCCA , CM000669.1:g.17332907_17332909delinsCCA GRCh37
NC_000007.12:g.17299432_17299434delinsCCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-3014_-202-3012delinsCCA ENSP00000495987.1:n.-202-3014_-202-3012delinsCCA
XR_927069.1:n.293+1881_293+1883delinsTGG
XR_927070.1:n.293+1881_293+1883delinsTGG
XR_927071.1:n.293+1881_293+1883delinsTGG
XR_927072.1:n.294+1881_294+1883delinsTGG
XR_927073.1:n.295+1881_295+1883delinsTGG
XR_927073.2:n.295+1881_295+1883delinsTGG