Canonical Allele Identifier: CA639173677
Gene: SSTR3 HGNC NCBI

Linked Data

dbSNP Id: rs1214614985

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37217294C>A , CM000684.2:g.37217294C>A GRCh38
NC_000022.10:g.37613334C>A , CM000684.1:g.37613334C>A GRCh37
NC_000022.9:g.35943280C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_005261721.3:c.-37+3113G>T XP_005261778.1:n.-37+3113G>T
XM_011530349.1:c.-694-1406G>T XP_011528651.1:n.-694-1406G>T
XM_005261721.4:c.-37+3113G>T XP_005261778.1:n.-37+3113G>T
XM_011530349.2:c.-694-1406G>T XP_011528651.1:n.-694-1406G>T
XM_017028924.1:c.-437-1406G>T XP_016884413.1:n.-437-1406G>T