Canonical Allele Identifier: CA2136094899

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199765C= , CM000676.2:g.50199765C=	GRCh38
NC_000014.8:g.50666483C= , CM000676.1:g.50666483C=	GRCh37
NC_000014.7:g.49736233C=	NCBI36
NG_051073.1:g.36929G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.436G= MANE Select	ENSP00000216373.5:p.Gly146=
ENST00000216373.9:c.436G=	ENSP00000216373.5:p.Gly146=
ENST00000543680.5:c.436G=	ENSP00000445328.1:p.Gly146=
ENST00000555666.1:n.615G=
ENST00000556469.5:n.407G=
NM_006939.2:c.436G=	NP_008870.2:p.Gly146=
XM_005268021.1:c.256G=	XP_005268078.1:p.Gly86=
XM_011537103.1:c.397G=	XP_011535405.1:p.Gly133=
XM_011537104.1:c.436G=	XP_011535406.1:p.Gly146=
XR_943842.1:n.1039+15893C=
XR_943843.1:n.1039+15893C=
NM_006939.3:c.436G=	NP_008870.2:p.Gly146=
NM_006939.4:c.436G= MANE Select	NP_008870.2:p.Gly146=