Canonical Allele Identifier: CA389644156

Gene: SOS2

Linked Data

• gnomAD v4: 14-50153105-A-G
• MyVariant Identifiers: chr14:g.50619823A>G (hg19) ; chr14:g.50153105A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153105A>G , CM000676.2:g.50153105A>G	GRCh38
NC_000014.8:g.50619823A>G , CM000676.1:g.50619823A>G	GRCh37
NC_000014.7:g.49689573A>G	NCBI36
NG_051073.1:g.83589T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2126T>C MANE Select	ENSP00000216373.5:p.Leu709Pro
ENST00000216373.9:c.2126T>C	ENSP00000216373.5:p.Leu709Pro
ENST00000543680.5:c.2027T>C	ENSP00000445328.1:p.Leu676Pro
NM_006939.2:c.2126T>C	NP_008870.2:p.Leu709Pro
XM_005268021.1:c.1946T>C	XP_005268078.1:p.Leu649Pro
XM_011537103.1:c.2087T>C	XP_011535405.1:p.Leu696Pro
XM_011537104.1:c.2126T>C	XP_011535406.1:p.Leu709Pro
NM_006939.3:c.2126T>C	NP_008870.2:p.Leu709Pro
NM_006939.4:c.2126T>C MANE Select	NP_008870.2:p.Leu709Pro