Canonical Allele Identifier: CA950579020
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1954583658
gnomAD v3: 12-93586119-G-A
gnomAD v4: 12-93586119-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586119G>A , CM000674.2:g.93586119G>A GRCh38
NC_000012.11:g.93979895G>A , CM000674.1:g.93979895G>A GRCh37
NC_000012.10:g.92504026G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005269213.3:c.*360G>A XP_005269270.2:n.*360G>A
XM_006719673.1:c.*360G>A XP_006719736.1:n.*360G>A
XM_006719674.1:c.*360G>A XP_006719737.1:n.*360G>A
XM_011538929.1:c.*360G>A XP_011537231.1:n.*360G>A
XM_011538930.1:c.*360G>A XP_011537232.1:n.*360G>A
XM_011538931.1:c.*360G>A XP_011537233.1:n.*360G>A
XM_011538932.1:c.*360G>A XP_011537234.1:n.*360G>A
XM_011538933.1:c.*360G>A XP_011537235.1:n.*360G>A
XM_011538934.1:c.*360G>A XP_011537236.1:n.*360G>A
XM_011538935.1:c.591+10946G>A XP_011537237.1:n.591+10946G>A
XR_944810.1:n.1704G>A
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