Canonical Allele Identifier: CA1691299000
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293510_17293511delinsTG , CM000669.2:g.17293510_17293511delinsTG GRCh38
NC_000007.13:g.17333134_17333135delinsTG , CM000669.1:g.17333134_17333135delinsTG GRCh37
NC_000007.12:g.17299659_17299660delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2787_-202-2786delinsTG ENSP00000495987.1:n.-202-2787_-202-2786delinsTG
XR_927069.1:n.293+1655_293+1656delinsCA
XR_927070.1:n.293+1655_293+1656delinsCA
XR_927071.1:n.293+1655_293+1656delinsCA
XR_927072.1:n.294+1655_294+1656delinsCA
XR_927073.1:n.295+1655_295+1656delinsCA
XR_927073.2:n.295+1655_295+1656delinsCA