Canonical Allele Identifier: CA2136084339

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180474A= , CM000676.2:g.50180474A=	GRCh38
NC_000014.8:g.50647192A= , CM000676.1:g.50647192A=	GRCh37
NC_000014.7:g.49716942A=	NCBI36
NG_051073.1:g.56220T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.969+98T= MANE Select	ENSP00000216373.5:n.969+98T=
ENST00000216373.9:c.969+98T=	ENSP00000216373.5:n.969+98T=
ENST00000543680.5:c.969+98T=	ENSP00000445328.1:n.969+98T=
ENST00000555794.2:c.83+98T=
NM_006939.2:c.969+98T=	NP_008870.2:n.969+98T=
XM_005268021.1:c.789+98T=	XP_005268078.1:n.789+98T=
XM_011537103.1:c.930+98T=	XP_011535405.1:n.930+98T=
XM_011537104.1:c.969+98T=	XP_011535406.1:n.969+98T=
XR_943842.1:n.954-3313A=
XR_943843.1:n.954-3313A=
NM_006939.3:c.969+98T=	NP_008870.2:n.969+98T=
NM_006939.4:c.969+98T= MANE Select	NP_008870.2:n.969+98T=