Canonical Allele Identifier: CA486174983

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50616860A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50150142A>G , CM000676.2:g.50150142A>G	GRCh38
NC_000014.8:g.50616860A>G , CM000676.1:g.50616860A>G	GRCh37
NC_000014.7:g.49686610A>G	NCBI36
NG_051073.1:g.86552T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2250T>C MANE Select	ENSP00000216373.5:p.Ile750=
ENST00000216373.9:c.2250T>C	ENSP00000216373.5:p.Ile750=
ENST00000543680.5:c.2151T>C	ENSP00000445328.1:p.Ile717=
NM_006939.2:c.2250T>C	NP_008870.2:p.Ile750=
XM_005268021.1:c.2070T>C	XP_005268078.1:p.Ile690=
XM_011537103.1:c.2211T>C	XP_011535405.1:p.Ile737=
XM_011537104.1:c.2250T>C	XP_011535406.1:p.Ile750=
NM_006939.3:c.2250T>C	NP_008870.2:p.Ile750=
NM_006939.4:c.2250T>C MANE Select	NP_008870.2:p.Ile750=