Canonical Allele Identifier: CA2136058837

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130597A= , CM000676.2:g.50130597A=	GRCh38
NC_000014.8:g.50597315A= , CM000676.1:g.50597315A=	GRCh37
NC_000014.7:g.49667065A=	NCBI36
NG_051073.1:g.106097T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3241T= MANE Select	ENSP00000216373.5:p.Ser1081=
ENST00000216373.9:c.3241T=	ENSP00000216373.5:p.Ser1081=
ENST00000543680.5:c.3142T=	ENSP00000445328.1:p.Ser1048=
NM_006939.2:c.3241T=	NP_008870.2:p.Ser1081=
XM_005268021.1:c.3061T=	XP_005268078.1:p.Ser1021=
XM_011537103.1:c.3202T=	XP_011535405.1:p.Ser1068=
NM_006939.3:c.3241T=	NP_008870.2:p.Ser1081=
NM_006939.4:c.3241T= MANE Select	NP_008870.2:p.Ser1081=