Canonical Allele Identifier: CA51878369
Gene:

Linked Data

dbSNP Id: rs386648209

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016352_88016394delinsCA , CM000664.2:g.88016352_88016394delinsCA GRCh38
NC_000002.11:g.88315871_88315913delinsCA , CM000664.1:g.88315871_88315913delinsCA GRCh37
NC_000002.10:g.88096986_88097028delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.697_739delinsCA
XR_940336.3:n.697_739delinsCA