Canonical Allele Identifier: CA693574700
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1267238678
MyVariant Identifiers: chr12:g.93979857G>A (hg19) chr12:g.93586081G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586081G>A , CM000674.2:g.93586081G>A GRCh38
NC_000012.11:g.93979857G>A , CM000674.1:g.93979857G>A GRCh37
NC_000012.10:g.92503988G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005269213.3:c.*322G>A XP_005269270.2:n.*322G>A
XM_006719673.1:c.*322G>A XP_006719736.1:n.*322G>A
XM_006719674.1:c.*322G>A XP_006719737.1:n.*322G>A
XM_011538929.1:c.*322G>A XP_011537231.1:n.*322G>A
XM_011538930.1:c.*322G>A XP_011537232.1:n.*322G>A
XM_011538931.1:c.*322G>A XP_011537233.1:n.*322G>A
XM_011538932.1:c.*322G>A XP_011537234.1:n.*322G>A
XM_011538933.1:c.*322G>A XP_011537235.1:n.*322G>A
XM_011538934.1:c.*322G>A XP_011537236.1:n.*322G>A
XM_011538935.1:c.591+10908G>A XP_011537237.1:n.591+10908G>A
XR_944810.1:n.1666G>A
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