Canonical Allele Identifier: CA693574633

Gene: SOCS2

Linked Data

• dbSNP Id: rs1307276523
• gnomAD v3: 12-93585946-TTAA-T
• gnomAD v4: 12-93585946-TTAA-T
• MyVariant Identifiers: chr12:g.93979723_93979725del (hg19) ; chr12:g.93585947_93585949del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93585952_93585954del , CM000674.2:g.93585952_93585954del	GRCh38
NC_000012.11:g.93979728_93979730del , CM000674.1:g.93979728_93979730del	GRCh37
NC_000012.10:g.92503859_92503861del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005269213.3:c.*193_*195del	XP_005269270.2:n.*193_*195del
XM_006719673.1:c.*193_*195del	XP_006719736.1:n.*193_*195del
XM_006719674.1:c.*193_*195del	XP_006719737.1:n.*193_*195del
XM_011538929.1:c.*193_*195del	XP_011537231.1:n.*193_*195del
XM_011538930.1:c.*193_*195del	XP_011537232.1:n.*193_*195del
XM_011538931.1:c.*193_*195del	XP_011537233.1:n.*193_*195del
XM_011538932.1:c.*193_*195del	XP_011537234.1:n.*193_*195del
XM_011538933.1:c.*193_*195del	XP_011537235.1:n.*193_*195del
XM_011538934.1:c.*193_*195del	XP_011537236.1:n.*193_*195del
XM_011538935.1:c.591+10779_591+10781del	XP_011537237.1:n.591+10779_591+10781del
XR_944810.1:n.1537_1539del