Canonical Allele Identifier: CA2136084662

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180643T= , CM000676.2:g.50180643T=	GRCh38
NC_000014.8:g.50647361T= , CM000676.1:g.50647361T=	GRCh37
NC_000014.7:g.49717111T=	NCBI36
NG_051073.1:g.56051A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.898A= MANE Select	ENSP00000216373.5:p.Ile300=
ENST00000216373.9:c.898A=	ENSP00000216373.5:p.Ile300=
ENST00000543680.5:c.898A=	ENSP00000445328.1:p.Ile300=
ENST00000555794.2:c.12A=
NM_006939.2:c.898A=	NP_008870.2:p.Ile300=
XM_005268021.1:c.718A=	XP_005268078.1:p.Ile240=
XM_011537103.1:c.859A=	XP_011535405.1:p.Ile287=
XM_011537104.1:c.898A=	XP_011535406.1:p.Ile300=
XR_943842.1:n.954-3144T=
XR_943843.1:n.954-3144T=
NM_006939.3:c.898A=	NP_008870.2:p.Ile300=
NM_006939.4:c.898A= MANE Select	NP_008870.2:p.Ile300=