Canonical Allele Identifier: CA486173147

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50666460C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199742C>A , CM000676.2:g.50199742C>A	GRCh38
NC_000014.8:g.50666460C>A , CM000676.1:g.50666460C>A	GRCh37
NC_000014.7:g.49736210C>A	NCBI36
NG_051073.1:g.36952G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.459G>T MANE Select	ENSP00000216373.5:p.Arg153=
ENST00000216373.9:c.459G>T	ENSP00000216373.5:p.Arg153=
ENST00000543680.5:c.459G>T	ENSP00000445328.1:p.Arg153=
ENST00000555666.1:n.638G>T
ENST00000556469.5:n.430G>T
NM_006939.2:c.459G>T	NP_008870.2:p.Arg153=
XM_005268021.1:c.279G>T	XP_005268078.1:p.Arg93=
XM_011537103.1:c.420G>T	XP_011535405.1:p.Arg140=
XM_011537104.1:c.459G>T	XP_011535406.1:p.Arg153=
XR_943842.1:n.1039+15870C>A
XR_943843.1:n.1039+15870C>A
NM_006939.3:c.459G>T	NP_008870.2:p.Arg153=
NM_006939.4:c.459G>T MANE Select	NP_008870.2:p.Arg153=