Canonical Allele Identifier: CA1691298885
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293399_17293400delinsTA , CM000669.2:g.17293399_17293400delinsTA GRCh38
NC_000007.13:g.17333023_17333024delinsTA , CM000669.1:g.17333023_17333024delinsTA GRCh37
NC_000007.12:g.17299548_17299549delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2898_-202-2897delinsTA ENSP00000495987.1:n.-202-2898_-202-2897delinsTA
XR_927069.1:n.293+1766_293+1767delinsTA
XR_927070.1:n.293+1766_293+1767delinsTA
XR_927071.1:n.293+1766_293+1767delinsTA
XR_927072.1:n.294+1766_294+1767delinsTA
XR_927073.1:n.295+1766_295+1767delinsTA
XR_927073.2:n.295+1766_295+1767delinsTA