Canonical Allele Identifier: CA2136058795

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130503C= , CM000676.2:g.50130503C=	GRCh38
NC_000014.8:g.50597221C= , CM000676.1:g.50597221C=	GRCh37
NC_000014.7:g.49666971C=	NCBI36
NG_051073.1:g.106191G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.3335G= MANE Select	ENSP00000216373.5:p.Cys1112=
ENST00000216373.9:c.3335G=	ENSP00000216373.5:p.Cys1112=
ENST00000543680.5:c.3236G=	ENSP00000445328.1:p.Cys1079=
NM_006939.2:c.3335G=	NP_008870.2:p.Cys1112=
XM_005268021.1:c.3155G=	XP_005268078.1:p.Cys1052=
XM_011537103.1:c.3296G=	XP_011535405.1:p.Cys1099=
NM_006939.3:c.3335G=	NP_008870.2:p.Cys1112=
NM_006939.4:c.3335G= MANE Select	NP_008870.2:p.Cys1112=