Canonical Allele Identifier: CA324069726
Gene: SSTR3 HGNC NCBI

Linked Data

dbSNP Id: rs185892584
gnomAD v2: 22-37613222-C-G
gnomAD v3: 22-37217182-C-G
gnomAD v4: 22-37217182-C-G
MyVariant Identifiers: chr22:g.37613222C>G (hg19) chr22:g.37217182C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37217182C>G , CM000684.2:g.37217182C>G GRCh38
NC_000022.10:g.37613222C>G , CM000684.1:g.37613222C>G GRCh37
NC_000022.9:g.35943168C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005261721.3:c.-37+3225G>C XP_005261778.1:n.-37+3225G>C
XM_011530349.1:c.-694-1294G>C XP_011528651.1:n.-694-1294G>C
XM_005261721.4:c.-37+3225G>C XP_005261778.1:n.-37+3225G>C
XM_011530349.2:c.-694-1294G>C XP_011528651.1:n.-694-1294G>C
XM_017028924.1:c.-437-1294G>C XP_016884413.1:n.-437-1294G>C
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