Canonical Allele Identifier: CA2255111820
Gene:

Linked Data

dbSNP Id: rs1907309257

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237143_30237144insT , CM000679.2:g.30237143_30237144insT GRCh38
NC_000017.10:g.28564161_28564162insT , CM000679.1:g.28564161_28564162insT GRCh37
NC_000017.9:g.25588287_25588288insT NCBI36
NG_011747.2:g.3793_3794insA

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+73_165+74insT
XR_001752824.1:n.280+73_280+74insT