Canonical Allele Identifier: CA2136094922

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199828G= , CM000676.2:g.50199828G=	GRCh38
NC_000014.8:g.50666546G= , CM000676.1:g.50666546G=	GRCh37
NC_000014.7:g.49736296G=	NCBI36
NG_051073.1:g.36866C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.373C= MANE Select	ENSP00000216373.5:p.His125=
ENST00000216373.9:c.373C=	ENSP00000216373.5:p.His125=
ENST00000543680.5:c.373C=	ENSP00000445328.1:p.His125=
ENST00000555666.1:n.552C=
ENST00000556469.5:n.344C=
NM_006939.2:c.373C=	NP_008870.2:p.His125=
XM_005268021.1:c.193C=	XP_005268078.1:p.His65=
XM_011537103.1:c.334C=	XP_011535405.1:p.His112=
XM_011537104.1:c.373C=	XP_011535406.1:p.His125=
XR_943842.1:n.1039+15956G=
XR_943843.1:n.1039+15956G=
NM_006939.3:c.373C=	NP_008870.2:p.His125=
NM_006939.4:c.373C= MANE Select	NP_008870.2:p.His125=