Canonical Allele Identifier: CA389640491

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597293G>C (hg19) ; chr14:g.50130575G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130575G>C , CM000676.2:g.50130575G>C	GRCh38
NC_000014.8:g.50597293G>C , CM000676.1:g.50597293G>C	GRCh37
NC_000014.7:g.49667043G>C	NCBI36
NG_051073.1:g.106119C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3263C>G MANE Select	ENSP00000216373.5:p.Thr1088Arg
ENST00000216373.9:c.3263C>G	ENSP00000216373.5:p.Thr1088Arg
ENST00000543680.5:c.3164C>G	ENSP00000445328.1:p.Thr1055Arg
NM_006939.2:c.3263C>G	NP_008870.2:p.Thr1088Arg
XM_005268021.1:c.3083C>G	XP_005268078.1:p.Thr1028Arg
XM_011537103.1:c.3224C>G	XP_011535405.1:p.Thr1075Arg
NM_006939.3:c.3263C>G	NP_008870.2:p.Thr1088Arg
NM_006939.4:c.3263C>G MANE Select	NP_008870.2:p.Thr1088Arg