Canonical Allele Identifier: CA486169579

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50647353T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50180635T>C , CM000676.2:g.50180635T>C	GRCh38
NC_000014.8:g.50647353T>C , CM000676.1:g.50647353T>C	GRCh37
NC_000014.7:g.49717103T>C	NCBI36
NG_051073.1:g.56059A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.906A>G MANE Select	ENSP00000216373.5:p.Ser302=
ENST00000216373.9:c.906A>G	ENSP00000216373.5:p.Ser302=
ENST00000543680.5:c.906A>G	ENSP00000445328.1:p.Ser302=
ENST00000555794.2:c.20A>G
NM_006939.2:c.906A>G	NP_008870.2:p.Ser302=
XM_005268021.1:c.726A>G	XP_005268078.1:p.Ser242=
XM_011537103.1:c.867A>G	XP_011535405.1:p.Ser289=
XM_011537104.1:c.906A>G	XP_011535406.1:p.Ser302=
XR_943842.1:n.954-3152T>C
XR_943843.1:n.954-3152T>C
NM_006939.3:c.906A>G	NP_008870.2:p.Ser302=
NM_006939.4:c.906A>G MANE Select	NP_008870.2:p.Ser302=