Canonical Allele Identifier: CA389640420

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597260T>C (hg19) ; chr14:g.50130542T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130542T>C , CM000676.2:g.50130542T>C	GRCh38
NC_000014.8:g.50597260T>C , CM000676.1:g.50597260T>C	GRCh37
NC_000014.7:g.49667010T>C	NCBI36
NG_051073.1:g.106152A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3296A>G MANE Select	ENSP00000216373.5:p.Asp1099Gly
ENST00000216373.9:c.3296A>G	ENSP00000216373.5:p.Asp1099Gly
ENST00000543680.5:c.3197A>G	ENSP00000445328.1:p.Asp1066Gly
NM_006939.2:c.3296A>G	NP_008870.2:p.Asp1099Gly
XM_005268021.1:c.3116A>G	XP_005268078.1:p.Asp1039Gly
XM_011537103.1:c.3257A>G	XP_011535405.1:p.Asp1086Gly
NM_006939.3:c.3296A>G	NP_008870.2:p.Asp1099Gly
NM_006939.4:c.3296A>G MANE Select	NP_008870.2:p.Asp1099Gly