Canonical Allele Identifier: CA2136094919

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199823T= , CM000676.2:g.50199823T=	GRCh38
NC_000014.8:g.50666541T= , CM000676.1:g.50666541T=	GRCh37
NC_000014.7:g.49736291T=	NCBI36
NG_051073.1:g.36871A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.378A= MANE Select	ENSP00000216373.5:p.Val126=
ENST00000216373.9:c.378A=	ENSP00000216373.5:p.Val126=
ENST00000543680.5:c.378A=	ENSP00000445328.1:p.Val126=
ENST00000555666.1:n.557A=
ENST00000556469.5:n.349A=
NM_006939.2:c.378A=	NP_008870.2:p.Val126=
XM_005268021.1:c.198A=	XP_005268078.1:p.Val66=
XM_011537103.1:c.339A=	XP_011535405.1:p.Val113=
XM_011537104.1:c.378A=	XP_011535406.1:p.Val126=
XR_943842.1:n.1039+15951T=
XR_943843.1:n.1039+15951T=
NM_006939.3:c.378A=	NP_008870.2:p.Val126=
NM_006939.4:c.378A= MANE Select	NP_008870.2:p.Val126=