Canonical Allele Identifier: CA7176851
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2835313
ClinVar RCV Id: RCV003755644
dbSNP Id: rs374654442
ExAC: 14:50597300 G / A
MyVariant Identifiers: chr14:g.50597300G>A (hg19) chr14:g.50130582G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130582G>A , CM000676.2:g.50130582G>A GRCh38
NC_000014.8:g.50597300G>A , CM000676.1:g.50597300G>A GRCh37
NC_000014.7:g.49667050G>A NCBI36
NG_051073.1:g.106112C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.3256C>T MANE Select ENSP00000216373.5:p.Pro1086Ser
ENST00000216373.9:c.3256C>T ENSP00000216373.5:p.Pro1086Ser
ENST00000543680.5:c.3157C>T ENSP00000445328.1:p.Pro1053Ser
NM_006939.2:c.3256C>T NP_008870.2:p.Pro1086Ser
XM_005268021.1:c.3076C>T XP_005268078.1:p.Pro1026Ser
XM_011537103.1:c.3217C>T XP_011535405.1:p.Pro1073Ser
NM_006939.3:c.3256C>T NP_008870.2:p.Pro1086Ser
NM_006939.4:c.3256C>T MANE Select NP_008870.2:p.Pro1086Ser
Search 100 bp 5'
Search 100 bp 3'