Canonical Allele Identifier: CA389640479

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597288A>G (hg19) ; chr14:g.50130570A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130570A>G , CM000676.2:g.50130570A>G	GRCh38
NC_000014.8:g.50597288A>G , CM000676.1:g.50597288A>G	GRCh37
NC_000014.7:g.49667038A>G	NCBI36
NG_051073.1:g.106124T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3268T>C MANE Select	ENSP00000216373.5:p.Ser1090Pro
ENST00000216373.9:c.3268T>C	ENSP00000216373.5:p.Ser1090Pro
ENST00000543680.5:c.3169T>C	ENSP00000445328.1:p.Ser1057Pro
NM_006939.2:c.3268T>C	NP_008870.2:p.Ser1090Pro
XM_005268021.1:c.3088T>C	XP_005268078.1:p.Ser1030Pro
XM_011537103.1:c.3229T>C	XP_011535405.1:p.Ser1077Pro
NM_006939.3:c.3268T>C	NP_008870.2:p.Ser1090Pro
NM_006939.4:c.3268T>C MANE Select	NP_008870.2:p.Ser1090Pro