Canonical Allele Identifier: CA486173173

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50666496A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199778A>T , CM000676.2:g.50199778A>T	GRCh38
NC_000014.8:g.50666496A>T , CM000676.1:g.50666496A>T	GRCh37
NC_000014.7:g.49736246A>T	NCBI36
NG_051073.1:g.36916T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.423T>A MANE Select	ENSP00000216373.5:p.Ile141=
ENST00000216373.9:c.423T>A	ENSP00000216373.5:p.Ile141=
ENST00000543680.5:c.423T>A	ENSP00000445328.1:p.Ile141=
ENST00000555666.1:n.602T>A
ENST00000556469.5:n.394T>A
NM_006939.2:c.423T>A	NP_008870.2:p.Ile141=
XM_005268021.1:c.243T>A	XP_005268078.1:p.Ile81=
XM_011537103.1:c.384T>A	XP_011535405.1:p.Ile128=
XM_011537104.1:c.423T>A	XP_011535406.1:p.Ile141=
XR_943842.1:n.1039+15906A>T
XR_943843.1:n.1039+15906A>T
NM_006939.3:c.423T>A	NP_008870.2:p.Ile141=
NM_006939.4:c.423T>A MANE Select	NP_008870.2:p.Ile141=