Canonical Allele Identifier: CA963009059

Gene: SOS2

Linked Data

• dbSNP Id: rs1885709885
• gnomAD v3: 14-50180842-CA-C
• gnomAD v4: 14-50180842-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180846del , CM000676.2:g.50180846del	GRCh38
NC_000014.8:g.50647564del , CM000676.1:g.50647564del	GRCh37
NC_000014.7:g.49717314del	NCBI36
NG_051073.1:g.55851del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-161del MANE Select	ENSP00000216373.5:n.859-161del
ENST00000216373.9:c.859-161del	ENSP00000216373.5:n.859-161del
ENST00000543680.5:c.859-161del	ENSP00000445328.1:n.859-161del
NM_006939.2:c.859-161del	NP_008870.2:n.859-161del
XM_005268021.1:c.679-161del	XP_005268078.1:n.679-161del
XM_011537103.1:c.820-161del	XP_011535405.1:n.820-161del
XM_011537104.1:c.859-161del	XP_011535406.1:n.859-161del
XR_943842.1:n.954-2941del
XR_943843.1:n.954-2941del
NM_006939.3:c.859-161del	NP_008870.2:n.859-161del
NM_006939.4:c.859-161del MANE Select	NP_008870.2:n.859-161del