Canonical Allele Identifier: CA242005071
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1026332449
gnomAD v3: 12-93586424-G-C
gnomAD v4: 12-93586424-G-C
MyVariant Identifiers: chr12:g.93980200G>C (hg19) chr12:g.93586424G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586424G>C , CM000674.2:g.93586424G>C GRCh38
NC_000012.11:g.93980200G>C , CM000674.1:g.93980200G>C GRCh37
NC_000012.10:g.92504331G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11251G>C XP_011537237.1:n.591+11251G>C
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