Canonical Allele Identifier: CA693573741

Gene: SOCS2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93583178A>T , CM000674.2:g.93583178A>T	GRCh38
NC_000012.11:g.93976954A>T , CM000674.1:g.93976954A>T	GRCh37
NC_000012.10:g.92501085A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000549510.1:c.272A>T
XM_005269213.3:c.592-2510A>T	XP_005269270.2:n.592-2510A>T
XM_006719673.1:c.592-2510A>T	XP_006719736.1:n.592-2510A>T
XM_006719674.1:c.592-2510A>T	XP_006719737.1:n.592-2510A>T
XM_011538929.1:c.592-2510A>T	XP_011537231.1:n.592-2510A>T
XM_011538930.1:c.592-2510A>T	XP_011537232.1:n.592-2510A>T
XM_011538931.1:c.592-2510A>T	XP_011537233.1:n.592-2510A>T
XM_011538932.1:c.592-2510A>T	XP_011537234.1:n.592-2510A>T
XM_011538933.1:c.592-2510A>T	XP_011537235.1:n.592-2510A>T
XM_011538934.1:c.592-2510A>T	XP_011537236.1:n.592-2510A>T
XM_011538935.1:c.591+8005A>T	XP_011537237.1:n.591+8005A>T
XM_011538936.1:c.*132A>T	XP_011537238.1:n.*132A>T
XR_944810.1:n.1162A>T