Canonical Allele Identifier: CA1691290815
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269590_17269606delinsATATCATCCCACACTCT , CM000669.2:g.17269590_17269606delinsATATCATCCCACACTCT GRCh38
NC_000007.13:g.17309214_17309230delinsATATCATCCCACACTCT , CM000669.1:g.17309214_17309230delinsATATCATCCCACACTCT GRCh37
NC_000007.12:g.17275739_17275755delinsATATCATCCCACACTCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-203+21864_-203+21880delinsATATCATCCCACACTCT ENSP00000495987.1:n.-203+21864_-203+21880delinsATATCATCCCACAC...
XR_927073.2:n.785-10278_785-10262delinsAGAGTGTGGGATGATAT