Canonical Allele Identifier: CA389640371

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597239A>G (hg19) ; chr14:g.50130521A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130521A>G , CM000676.2:g.50130521A>G	GRCh38
NC_000014.8:g.50597239A>G , CM000676.1:g.50597239A>G	GRCh37
NC_000014.7:g.49666989A>G	NCBI36
NG_051073.1:g.106173T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3317T>C MANE Select	ENSP00000216373.5:p.Val1106Ala
ENST00000216373.9:c.3317T>C	ENSP00000216373.5:p.Val1106Ala
ENST00000543680.5:c.3218T>C	ENSP00000445328.1:p.Val1073Ala
NM_006939.2:c.3317T>C	NP_008870.2:p.Val1106Ala
XM_005268021.1:c.3137T>C	XP_005268078.1:p.Val1046Ala
XM_011537103.1:c.3278T>C	XP_011535405.1:p.Val1093Ala
NM_006939.3:c.3317T>C	NP_008870.2:p.Val1106Ala
NM_006939.4:c.3317T>C MANE Select	NP_008870.2:p.Val1106Ala