Canonical Allele Identifier: CA324069873
Gene: SSTR3 HGNC NCBI

Linked Data

dbSNP Id: rs565114641

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37217367C>T , CM000684.2:g.37217367C>T GRCh38
NC_000022.10:g.37613407C>T , CM000684.1:g.37613407C>T GRCh37
NC_000022.9:g.35943353C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005261721.3:c.-37+3040G>A XP_005261778.1:n.-37+3040G>A
XM_011530349.1:c.-694-1479G>A XP_011528651.1:n.-694-1479G>A
XM_005261721.4:c.-37+3040G>A XP_005261778.1:n.-37+3040G>A
XM_011530349.2:c.-694-1479G>A XP_011528651.1:n.-694-1479G>A
XM_017028924.1:c.-437-1479G>A XP_016884413.1:n.-437-1479G>A