Canonical Allele Identifier: CA389640327

Gene: SOS2

Linked Data

• dbSNP Id: rs1883833742
• MyVariant Identifiers: chr14:g.50597219C>T (hg19) ; chr14:g.50130501C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130501C>T , CM000676.2:g.50130501C>T	GRCh38
NC_000014.8:g.50597219C>T , CM000676.1:g.50597219C>T	GRCh37
NC_000014.7:g.49666969C>T	NCBI36
NG_051073.1:g.106193G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.3337G>A MANE Select	ENSP00000216373.5:p.Gly1113Ser
ENST00000216373.9:c.3337G>A	ENSP00000216373.5:p.Gly1113Ser
ENST00000543680.5:c.3238G>A	ENSP00000445328.1:p.Gly1080Ser
NM_006939.2:c.3337G>A	NP_008870.2:p.Gly1113Ser
XM_005268021.1:c.3157G>A	XP_005268078.1:p.Gly1053Ser
XM_011537103.1:c.3298G>A	XP_011535405.1:p.Gly1100Ser
NM_006939.3:c.3337G>A	NP_008870.2:p.Gly1113Ser
NM_006939.4:c.3337G>A MANE Select	NP_008870.2:p.Gly1113Ser