Canonical Allele Identifier: CA2136084666

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180649G= , CM000676.2:g.50180649G=	GRCh38
NC_000014.8:g.50647367G= , CM000676.1:g.50647367G=	GRCh37
NC_000014.7:g.49717117G=	NCBI36
NG_051073.1:g.56045C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.892C= MANE Select	ENSP00000216373.5:p.Gln298=
ENST00000216373.9:c.892C=	ENSP00000216373.5:p.Gln298=
ENST00000543680.5:c.892C=	ENSP00000445328.1:p.Gln298=
ENST00000555794.2:c.6C=
NM_006939.2:c.892C=	NP_008870.2:p.Gln298=
XM_005268021.1:c.712C=	XP_005268078.1:p.Gln238=
XM_011537103.1:c.853C=	XP_011535405.1:p.Gln285=
XM_011537104.1:c.892C=	XP_011535406.1:p.Gln298=
XR_943842.1:n.954-3138G=
XR_943843.1:n.954-3138G=
NM_006939.3:c.892C=	NP_008870.2:p.Gln298=
NM_006939.4:c.892C= MANE Select	NP_008870.2:p.Gln298=