Canonical Allele Identifier: CA963009085

Gene: SOS2

Linked Data

• dbSNP Id: rs1885712695
• gnomAD v3: 14-50180877-AGAG-A
• gnomAD v4: 14-50180877-AGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180878_50180880del , CM000676.2:g.50180878_50180880del	GRCh38
NC_000014.8:g.50647596_50647598del , CM000676.1:g.50647596_50647598del	GRCh37
NC_000014.7:g.49717346_49717348del	NCBI36
NG_051073.1:g.55814_55816del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-198_859-196del MANE Select	ENSP00000216373.5:n.859-198_859-196del
ENST00000216373.9:c.859-198_859-196del	ENSP00000216373.5:n.859-198_859-196del
ENST00000543680.5:c.859-198_859-196del	ENSP00000445328.1:n.859-198_859-196del
NM_006939.2:c.859-198_859-196del	NP_008870.2:n.859-198_859-196del
XM_005268021.1:c.679-198_679-196del	XP_005268078.1:n.679-198_679-196del
XM_011537103.1:c.820-198_820-196del	XP_011535405.1:n.820-198_820-196del
XM_011537104.1:c.859-198_859-196del	XP_011535406.1:n.859-198_859-196del
XR_943842.1:n.954-2909_954-2907del
XR_943843.1:n.954-2909_954-2907del
NM_006939.3:c.859-198_859-196del	NP_008870.2:n.859-198_859-196del
NM_006939.4:c.859-198_859-196del MANE Select	NP_008870.2:n.859-198_859-196del