Canonical Allele Identifier: CA1691298848
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293370_17293374delinsAAGTC , CM000669.2:g.17293370_17293374delinsAAGTC GRCh38
NC_000007.13:g.17332994_17332998delinsAAGTC , CM000669.1:g.17332994_17332998delinsAAGTC GRCh37
NC_000007.12:g.17299519_17299523delinsAAGTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2927_-202-2923delinsAAGTC ENSP00000495987.1:n.-202-2927_-202-2923delinsAAGTC
XR_927069.1:n.293+1792_293+1796delinsGACTT
XR_927070.1:n.293+1792_293+1796delinsGACTT
XR_927071.1:n.293+1792_293+1796delinsGACTT
XR_927072.1:n.294+1792_294+1796delinsGACTT
XR_927073.1:n.295+1792_295+1796delinsGACTT
XR_927073.2:n.295+1792_295+1796delinsGACTT