Canonical Allele Identifier: CA2136084643

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180624T= , CM000676.2:g.50180624T=	GRCh38
NC_000014.8:g.50647342T= , CM000676.1:g.50647342T=	GRCh37
NC_000014.7:g.49717092T=	NCBI36
NG_051073.1:g.56070A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.917A= MANE Select	ENSP00000216373.5:p.His306=
ENST00000216373.9:c.917A=	ENSP00000216373.5:p.His306=
ENST00000543680.5:c.917A=	ENSP00000445328.1:p.His306=
ENST00000555794.2:c.31A=
NM_006939.2:c.917A=	NP_008870.2:p.His306=
XM_005268021.1:c.737A=	XP_005268078.1:p.His246=
XM_011537103.1:c.878A=	XP_011535405.1:p.His293=
XM_011537104.1:c.917A=	XP_011535406.1:p.His306=
XR_943842.1:n.954-3163T=
XR_943843.1:n.954-3163T=
NM_006939.3:c.917A=	NP_008870.2:p.His306=
NM_006939.4:c.917A= MANE Select	NP_008870.2:p.His306=