Canonical Allele Identifier: CA389640326

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597219C>G (hg19) ; chr14:g.50130501C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.3337G>C MANE Select	ENSP00000216373.5:p.Gly1113Arg
ENST00000216373.9:c.3337G>C	ENSP00000216373.5:p.Gly1113Arg
ENST00000543680.5:c.3238G>C	ENSP00000445328.1:p.Gly1080Arg
NM_006939.2:c.3337G>C	NP_008870.2:p.Gly1113Arg
XM_005268021.1:c.3157G>C	XP_005268078.1:p.Gly1053Arg
XM_011537103.1:c.3298G>C	XP_011535405.1:p.Gly1100Arg
NM_006939.3:c.3337G>C	NP_008870.2:p.Gly1113Arg
NM_006939.4:c.3337G>C MANE Select	NP_008870.2:p.Gly1113Arg