Canonical Allele Identifier: CA389640601

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597320G>C (hg19) ; chr14:g.50130602G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130602G>C , CM000676.2:g.50130602G>C	GRCh38
NC_000014.8:g.50597320G>C , CM000676.1:g.50597320G>C	GRCh37
NC_000014.7:g.49667070G>C	NCBI36
NG_051073.1:g.106092C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3236C>G MANE Select	ENSP00000216373.5:p.Thr1079Arg
ENST00000216373.9:c.3236C>G	ENSP00000216373.5:p.Thr1079Arg
ENST00000543680.5:c.3137C>G	ENSP00000445328.1:p.Thr1046Arg
NM_006939.2:c.3236C>G	NP_008870.2:p.Thr1079Arg
XM_005268021.1:c.3056C>G	XP_005268078.1:p.Thr1019Arg
XM_011537103.1:c.3197C>G	XP_011535405.1:p.Thr1066Arg
NM_006939.3:c.3236C>G	NP_008870.2:p.Thr1079Arg
NM_006939.4:c.3236C>G MANE Select	NP_008870.2:p.Thr1079Arg