Canonical Allele Identifier: CA324069901
Gene: SSTR3 HGNC NCBI

Linked Data

dbSNP Id: rs763667585

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37217425del , CM000684.2:g.37217425del GRCh38
NC_000022.10:g.37613465del , CM000684.1:g.37613465del GRCh37
NC_000022.9:g.35943411del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005261721.3:c.-37+2986del XP_005261778.1:n.-37+2986del
XM_011530349.1:c.-694-1533del XP_011528651.1:n.-694-1533del
XM_005261721.4:c.-37+2986del XP_005261778.1:n.-37+2986del
XM_011530349.2:c.-694-1533del XP_011528651.1:n.-694-1533del
XM_017028924.1:c.-437-1533del XP_016884413.1:n.-437-1533del