Canonical Allele Identifier: CA389644231

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50619853A>T (hg19) ; chr14:g.50153135A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153135A>T , CM000676.2:g.50153135A>T	GRCh38
NC_000014.8:g.50619853A>T , CM000676.1:g.50619853A>T	GRCh37
NC_000014.7:g.49689603A>T	NCBI36
NG_051073.1:g.83559T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.2096T>A MANE Select	ENSP00000216373.5:p.Phe699Tyr
ENST00000216373.9:c.2096T>A	ENSP00000216373.5:p.Phe699Tyr
ENST00000543680.5:c.1997T>A	ENSP00000445328.1:p.Phe666Tyr
NM_006939.2:c.2096T>A	NP_008870.2:p.Phe699Tyr
XM_005268021.1:c.1916T>A	XP_005268078.1:p.Phe639Tyr
XM_011537103.1:c.2057T>A	XP_011535405.1:p.Phe686Tyr
XM_011537104.1:c.2096T>A	XP_011535406.1:p.Phe699Tyr
NM_006939.3:c.2096T>A	NP_008870.2:p.Phe699Tyr
NM_006939.4:c.2096T>A MANE Select	NP_008870.2:p.Phe699Tyr