Canonical Allele Identifier: CA2136084798

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180795A= , CM000676.2:g.50180795A=	GRCh38
NC_000014.8:g.50647513A= , CM000676.1:g.50647513A=	GRCh37
NC_000014.7:g.49717263A=	NCBI36
NG_051073.1:g.55899T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.859-113T= MANE Select	ENSP00000216373.5:n.859-113T=
ENST00000216373.9:c.859-113T=	ENSP00000216373.5:n.859-113T=
ENST00000543680.5:c.859-113T=	ENSP00000445328.1:n.859-113T=
NM_006939.2:c.859-113T=	NP_008870.2:n.859-113T=
XM_005268021.1:c.679-113T=	XP_005268078.1:n.679-113T=
XM_011537103.1:c.820-113T=	XP_011535405.1:n.820-113T=
XM_011537104.1:c.859-113T=	XP_011535406.1:n.859-113T=
XR_943842.1:n.954-2992A=
XR_943843.1:n.954-2992A=
NM_006939.3:c.859-113T=	NP_008870.2:n.859-113T=
NM_006939.4:c.859-113T= MANE Select	NP_008870.2:n.859-113T=