Canonical Allele Identifier: CA486173079

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597268A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130550A>C , CM000676.2:g.50130550A>C	GRCh38
NC_000014.8:g.50597268A>C , CM000676.1:g.50597268A>C	GRCh37
NC_000014.7:g.49667018A>C	NCBI36
NG_051073.1:g.106144T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3288T>G MANE Select	ENSP00000216373.5:p.Ala1096=
ENST00000216373.9:c.3288T>G	ENSP00000216373.5:p.Ala1096=
ENST00000543680.5:c.3189T>G	ENSP00000445328.1:p.Ala1063=
NM_006939.2:c.3288T>G	NP_008870.2:p.Ala1096=
XM_005268021.1:c.3108T>G	XP_005268078.1:p.Ala1036=
XM_011537103.1:c.3249T>G	XP_011535405.1:p.Ala1083=
NM_006939.3:c.3288T>G	NP_008870.2:p.Ala1096=
NM_006939.4:c.3288T>G MANE Select	NP_008870.2:p.Ala1096=