Canonical Allele Identifier: CA2136094892

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199742C= , CM000676.2:g.50199742C=	GRCh38
NC_000014.8:g.50666460C= , CM000676.1:g.50666460C=	GRCh37
NC_000014.7:g.49736210C=	NCBI36
NG_051073.1:g.36952G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.459G= MANE Select	ENSP00000216373.5:p.Arg153=
ENST00000216373.9:c.459G=	ENSP00000216373.5:p.Arg153=
ENST00000543680.5:c.459G=	ENSP00000445328.1:p.Arg153=
ENST00000555666.1:n.638G=
ENST00000556469.5:n.430G=
NM_006939.2:c.459G=	NP_008870.2:p.Arg153=
XM_005268021.1:c.279G=	XP_005268078.1:p.Arg93=
XM_011537103.1:c.420G=	XP_011535405.1:p.Arg140=
XM_011537104.1:c.459G=	XP_011535406.1:p.Arg153=
XR_943842.1:n.1039+15870C=
XR_943843.1:n.1039+15870C=
NM_006939.3:c.459G=	NP_008870.2:p.Arg153=
NM_006939.4:c.459G= MANE Select	NP_008870.2:p.Arg153=