Canonical Allele Identifier: CA2136084830

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180834C= , CM000676.2:g.50180834C=	GRCh38
NC_000014.8:g.50647552C= , CM000676.1:g.50647552C=	GRCh37
NC_000014.7:g.49717302C=	NCBI36
NG_051073.1:g.55860G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-152G= MANE Select	ENSP00000216373.5:n.859-152G=
ENST00000216373.9:c.859-152G=	ENSP00000216373.5:n.859-152G=
ENST00000543680.5:c.859-152G=	ENSP00000445328.1:n.859-152G=
NM_006939.2:c.859-152G=	NP_008870.2:n.859-152G=
XM_005268021.1:c.679-152G=	XP_005268078.1:n.679-152G=
XM_011537103.1:c.820-152G=	XP_011535405.1:n.820-152G=
XM_011537104.1:c.859-152G=	XP_011535406.1:n.859-152G=
XR_943842.1:n.954-2953C=
XR_943843.1:n.954-2953C=
NM_006939.3:c.859-152G=	NP_008870.2:n.859-152G=
NM_006939.4:c.859-152G= MANE Select	NP_008870.2:n.859-152G=