Canonical Allele Identifier: CA2136084383

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180521T= , CM000676.2:g.50180521T=	GRCh38
NC_000014.8:g.50647239T= , CM000676.1:g.50647239T=	GRCh37
NC_000014.7:g.49716989T=	NCBI36
NG_051073.1:g.56173A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.969+51A= MANE Select	ENSP00000216373.5:n.969+51A=
ENST00000216373.9:c.969+51A=	ENSP00000216373.5:n.969+51A=
ENST00000543680.5:c.969+51A=	ENSP00000445328.1:n.969+51A=
ENST00000555794.2:c.83+51A=
NM_006939.2:c.969+51A=	NP_008870.2:n.969+51A=
XM_005268021.1:c.789+51A=	XP_005268078.1:n.789+51A=
XM_011537103.1:c.930+51A=	XP_011535405.1:n.930+51A=
XM_011537104.1:c.969+51A=	XP_011535406.1:n.969+51A=
XR_943842.1:n.954-3266T=
XR_943843.1:n.954-3266T=
NM_006939.3:c.969+51A=	NP_008870.2:n.969+51A=
NM_006939.4:c.969+51A= MANE Select	NP_008870.2:n.969+51A=