Canonical Allele Identifier: CA2136086398

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50182437G= , CM000676.2:g.50182437G=	GRCh38
NC_000014.8:g.50649155G= , CM000676.1:g.50649155G=	GRCh37
NC_000014.7:g.49718905G=	NCBI36
NG_051073.1:g.54257C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.858+26C= MANE Select	ENSP00000216373.5:n.858+26C=
ENST00000216373.9:c.858+26C=	ENSP00000216373.5:n.858+26C=
ENST00000543680.5:c.858+26C=	ENSP00000445328.1:n.858+26C=
NM_006939.2:c.858+26C=	NP_008870.2:n.858+26C=
XM_005268021.1:c.678+26C=	XP_005268078.1:n.678+26C=
XM_011537103.1:c.819+26C=	XP_011535405.1:n.819+26C=
XM_011537104.1:c.858+26C=	XP_011535406.1:n.858+26C=
XR_943842.1:n.954-1350G=
XR_943843.1:n.954-1350G=
NM_006939.3:c.858+26C=	NP_008870.2:n.858+26C=
NM_006939.4:c.858+26C= MANE Select	NP_008870.2:n.858+26C=