Canonical Allele Identifier: CA260721598

Gene: SOS2

Linked Data

• ClinVar Variation Id: 639276
• ClinVar RCV Id: RCV000792030 ; RCV002332581
• dbSNP Id: rs1051166055
• MyVariant Identifiers: chr14:g.50666487C>T (hg19) ; chr14:g.50199769C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199769C>T , CM000676.2:g.50199769C>T	GRCh38
NC_000014.8:g.50666487C>T , CM000676.1:g.50666487C>T	GRCh37
NC_000014.7:g.49736237C>T	NCBI36
NG_051073.1:g.36925G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.432G>A MANE Select	ENSP00000216373.5:p.Leu144=
ENST00000216373.9:c.432G>A	ENSP00000216373.5:p.Leu144=
ENST00000543680.5:c.432G>A	ENSP00000445328.1:p.Leu144=
ENST00000555666.1:n.611G>A
ENST00000556469.5:n.403G>A
NM_006939.2:c.432G>A	NP_008870.2:p.Leu144=
XM_005268021.1:c.252G>A	XP_005268078.1:p.Leu84=
XM_011537103.1:c.393G>A	XP_011535405.1:p.Leu131=
XM_011537104.1:c.432G>A	XP_011535406.1:p.Leu144=
XR_943842.1:n.1039+15897C>T
XR_943843.1:n.1039+15897C>T
NM_006939.3:c.432G>A	NP_008870.2:p.Leu144=
NM_006939.4:c.432G>A MANE Select	NP_008870.2:p.Leu144=