Canonical Allele Identifier: CA486173248

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597313T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130595T>G , CM000676.2:g.50130595T>G	GRCh38
NC_000014.8:g.50597313T>G , CM000676.1:g.50597313T>G	GRCh37
NC_000014.7:g.49667063T>G	NCBI36
NG_051073.1:g.106099A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3243A>C MANE Select	ENSP00000216373.5:p.Ser1081=
ENST00000216373.9:c.3243A>C	ENSP00000216373.5:p.Ser1081=
ENST00000543680.5:c.3144A>C	ENSP00000445328.1:p.Ser1048=
NM_006939.2:c.3243A>C	NP_008870.2:p.Ser1081=
XM_005268021.1:c.3063A>C	XP_005268078.1:p.Ser1021=
XM_011537103.1:c.3204A>C	XP_011535405.1:p.Ser1068=
NM_006939.3:c.3243A>C	NP_008870.2:p.Ser1081=
NM_006939.4:c.3243A>C MANE Select	NP_008870.2:p.Ser1081=