Canonical Allele Identifier: CA752891013
Gene: SSTR3 HGNC NCBI

Linked Data

dbSNP Id: rs1210904910
MyVariant Identifiers: chr22:g.37613422A>T (hg19) chr22:g.37217382A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37217382A>T , CM000684.2:g.37217382A>T GRCh38
NC_000022.10:g.37613422A>T , CM000684.1:g.37613422A>T GRCh37
NC_000022.9:g.35943368A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005261721.3:c.-37+3025T>A XP_005261778.1:n.-37+3025T>A
XM_011530349.1:c.-694-1494T>A XP_011528651.1:n.-694-1494T>A
XM_005261721.4:c.-37+3025T>A XP_005261778.1:n.-37+3025T>A
XM_011530349.2:c.-694-1494T>A XP_011528651.1:n.-694-1494T>A
XM_017028924.1:c.-437-1494T>A XP_016884413.1:n.-437-1494T>A
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