Canonical Allele Identifier: CA486173152

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50666463G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199745G>A , CM000676.2:g.50199745G>A	GRCh38
NC_000014.8:g.50666463G>A , CM000676.1:g.50666463G>A	GRCh37
NC_000014.7:g.49736213G>A	NCBI36
NG_051073.1:g.36949C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.456C>T MANE Select	ENSP00000216373.5:p.Ile152=
ENST00000216373.9:c.456C>T	ENSP00000216373.5:p.Ile152=
ENST00000543680.5:c.456C>T	ENSP00000445328.1:p.Ile152=
ENST00000555666.1:n.635C>T
ENST00000556469.5:n.427C>T
NM_006939.2:c.456C>T	NP_008870.2:p.Ile152=
XM_005268021.1:c.276C>T	XP_005268078.1:p.Ile92=
XM_011537103.1:c.417C>T	XP_011535405.1:p.Ile139=
XM_011537104.1:c.456C>T	XP_011535406.1:p.Ile152=
XR_943842.1:n.1039+15873G>A
XR_943843.1:n.1039+15873G>A
NM_006939.3:c.456C>T	NP_008870.2:p.Ile152=
NM_006939.4:c.456C>T MANE Select	NP_008870.2:p.Ile152=