Canonical Allele Identifier: CA486173191

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50666526C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199808C>T , CM000676.2:g.50199808C>T	GRCh38
NC_000014.8:g.50666526C>T , CM000676.1:g.50666526C>T	GRCh37
NC_000014.7:g.49736276C>T	NCBI36
NG_051073.1:g.36886G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.393G>A MANE Select	ENSP00000216373.5:p.Val131=
ENST00000216373.9:c.393G>A	ENSP00000216373.5:p.Val131=
ENST00000543680.5:c.393G>A	ENSP00000445328.1:p.Val131=
ENST00000555666.1:n.572G>A
ENST00000556469.5:n.364G>A
NM_006939.2:c.393G>A	NP_008870.2:p.Val131=
XM_005268021.1:c.213G>A	XP_005268078.1:p.Val71=
XM_011537103.1:c.354G>A	XP_011535405.1:p.Val118=
XM_011537104.1:c.393G>A	XP_011535406.1:p.Val131=
XR_943842.1:n.1039+15936C>T
XR_943843.1:n.1039+15936C>T
NM_006939.3:c.393G>A	NP_008870.2:p.Val131=
NM_006939.4:c.393G>A MANE Select	NP_008870.2:p.Val131=