Canonical Allele Identifier: CA2136058794

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130501C= , CM000676.2:g.50130501C=	GRCh38
NC_000014.8:g.50597219C= , CM000676.1:g.50597219C=	GRCh37
NC_000014.7:g.49666969C=	NCBI36
NG_051073.1:g.106193G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.3337G= MANE Select	ENSP00000216373.5:p.Gly1113=
ENST00000216373.9:c.3337G=	ENSP00000216373.5:p.Gly1113=
ENST00000543680.5:c.3238G=	ENSP00000445328.1:p.Gly1080=
NM_006939.2:c.3337G=	NP_008870.2:p.Gly1113=
XM_005268021.1:c.3157G=	XP_005268078.1:p.Gly1053=
XM_011537103.1:c.3298G=	XP_011535405.1:p.Gly1100=
NM_006939.3:c.3337G=	NP_008870.2:p.Gly1113=
NM_006939.4:c.3337G= MANE Select	NP_008870.2:p.Gly1113=