Canonical Allele Identifier: CA486173096

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597283A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130565A>C , CM000676.2:g.50130565A>C	GRCh38
NC_000014.8:g.50597283A>C , CM000676.1:g.50597283A>C	GRCh37
NC_000014.7:g.49667033A>C	NCBI36
NG_051073.1:g.106129T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3273T>G MANE Select	ENSP00000216373.5:p.Thr1091=
ENST00000216373.9:c.3273T>G	ENSP00000216373.5:p.Thr1091=
ENST00000543680.5:c.3174T>G	ENSP00000445328.1:p.Thr1058=
NM_006939.2:c.3273T>G	NP_008870.2:p.Thr1091=
XM_005268021.1:c.3093T>G	XP_005268078.1:p.Thr1031=
XM_011537103.1:c.3234T>G	XP_011535405.1:p.Thr1078=
NM_006939.3:c.3273T>G	NP_008870.2:p.Thr1091=
NM_006939.4:c.3273T>G MANE Select	NP_008870.2:p.Thr1091=