Canonical Allele Identifier: CA486175143

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50619858A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153140A>G , CM000676.2:g.50153140A>G	GRCh38
NC_000014.8:g.50619858A>G , CM000676.1:g.50619858A>G	GRCh37
NC_000014.7:g.49689608A>G	NCBI36
NG_051073.1:g.83554T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2091T>C MANE Select	ENSP00000216373.5:p.His697=
ENST00000216373.9:c.2091T>C	ENSP00000216373.5:p.His697=
ENST00000543680.5:c.1992T>C	ENSP00000445328.1:p.His664=
NM_006939.2:c.2091T>C	NP_008870.2:p.His697=
XM_005268021.1:c.1911T>C	XP_005268078.1:p.His637=
XM_011537103.1:c.2052T>C	XP_011535405.1:p.His684=
XM_011537104.1:c.2091T>C	XP_011535406.1:p.His697=
NM_006939.3:c.2091T>C	NP_008870.2:p.His697=
NM_006939.4:c.2091T>C MANE Select	NP_008870.2:p.His697=