Canonical Allele Identifier: CA486174995

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50616881T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50150163T>A , CM000676.2:g.50150163T>A	GRCh38
NC_000014.8:g.50616881T>A , CM000676.1:g.50616881T>A	GRCh37
NC_000014.7:g.49686631T>A	NCBI36
NG_051073.1:g.86531A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2229A>T MANE Select	ENSP00000216373.5:p.Ala743=
ENST00000216373.9:c.2229A>T	ENSP00000216373.5:p.Ala743=
ENST00000543680.5:c.2130A>T	ENSP00000445328.1:p.Ala710=
NM_006939.2:c.2229A>T	NP_008870.2:p.Ala743=
XM_005268021.1:c.2049A>T	XP_005268078.1:p.Ala683=
XM_011537103.1:c.2190A>T	XP_011535405.1:p.Ala730=
XM_011537104.1:c.2229A>T	XP_011535406.1:p.Ala743=
NM_006939.3:c.2229A>T	NP_008870.2:p.Ala743=
NM_006939.4:c.2229A>T MANE Select	NP_008870.2:p.Ala743=