Canonical Allele Identifier: CA486169547

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50647347C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180629C>T , CM000676.2:g.50180629C>T	GRCh38
NC_000014.8:g.50647347C>T , CM000676.1:g.50647347C>T	GRCh37
NC_000014.7:g.49717097C>T	NCBI36
NG_051073.1:g.56065G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.912G>A MANE Select	ENSP00000216373.5:p.Glu304=
ENST00000216373.9:c.912G>A	ENSP00000216373.5:p.Glu304=
ENST00000543680.5:c.912G>A	ENSP00000445328.1:p.Glu304=
ENST00000555794.2:c.26G>A
NM_006939.2:c.912G>A	NP_008870.2:p.Glu304=
XM_005268021.1:c.732G>A	XP_005268078.1:p.Glu244=
XM_011537103.1:c.873G>A	XP_011535405.1:p.Glu291=
XM_011537104.1:c.912G>A	XP_011535406.1:p.Glu304=
XR_943842.1:n.954-3158C>T
XR_943843.1:n.954-3158C>T
NM_006939.3:c.912G>A	NP_008870.2:p.Glu304=
NM_006939.4:c.912G>A MANE Select	NP_008870.2:p.Glu304=