Canonical Allele Identifier: CA2136058809

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130535A= , CM000676.2:g.50130535A=	GRCh38
NC_000014.8:g.50597253A= , CM000676.1:g.50597253A=	GRCh37
NC_000014.7:g.49667003A=	NCBI36
NG_051073.1:g.106159T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3303T= MANE Select	ENSP00000216373.5:p.Ser1101=
ENST00000216373.9:c.3303T=	ENSP00000216373.5:p.Ser1101=
ENST00000543680.5:c.3204T=	ENSP00000445328.1:p.Ser1068=
NM_006939.2:c.3303T=	NP_008870.2:p.Ser1101=
XM_005268021.1:c.3123T=	XP_005268078.1:p.Ser1041=
XM_011537103.1:c.3264T=	XP_011535405.1:p.Ser1088=
NM_006939.3:c.3303T=	NP_008870.2:p.Ser1101=
NM_006939.4:c.3303T= MANE Select	NP_008870.2:p.Ser1101=