Canonical Allele Identifier: CA606966582

Gene: SOCS2

Linked Data

• gnomAD v2: 12-93979834-TCCCCCAAA-T
• MyVariant Identifiers: chr12:g.93979835_93979842del (hg19) ; chr12:g.93586059_93586066del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586059_93586066del , CM000674.2:g.93586059_93586066del	GRCh38
NC_000012.11:g.93979835_93979842del , CM000674.1:g.93979835_93979842del	GRCh37
NC_000012.10:g.92503966_92503973del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005269213.3:c.*300_*307del	XP_005269270.2:n.*300_*307del
XM_006719673.1:c.*300_*307del	XP_006719736.1:n.*300_*307del
XM_006719674.1:c.*300_*307del	XP_006719737.1:n.*300_*307del
XM_011538929.1:c.*300_*307del	XP_011537231.1:n.*300_*307del
XM_011538930.1:c.*300_*307del	XP_011537232.1:n.*300_*307del
XM_011538931.1:c.*300_*307del	XP_011537233.1:n.*300_*307del
XM_011538932.1:c.*300_*307del	XP_011537234.1:n.*300_*307del
XM_011538933.1:c.*300_*307del	XP_011537235.1:n.*300_*307del
XM_011538934.1:c.*300_*307del	XP_011537236.1:n.*300_*307del
XM_011538935.1:c.591+10886_591+10893del	XP_011537237.1:n.591+10886_591+10893del
XR_944810.1:n.1644_1651del