Canonical Allele Identifier: CA486173255

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50597319T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130601T>G , CM000676.2:g.50130601T>G	GRCh38
NC_000014.8:g.50597319T>G , CM000676.1:g.50597319T>G	GRCh37
NC_000014.7:g.49667069T>G	NCBI36
NG_051073.1:g.106093A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3237A>C MANE Select	ENSP00000216373.5:p.Thr1079=
ENST00000216373.9:c.3237A>C	ENSP00000216373.5:p.Thr1079=
ENST00000543680.5:c.3138A>C	ENSP00000445328.1:p.Thr1046=
NM_006939.2:c.3237A>C	NP_008870.2:p.Thr1079=
XM_005268021.1:c.3057A>C	XP_005268078.1:p.Thr1019=
XM_011537103.1:c.3198A>C	XP_011535405.1:p.Thr1066=
NM_006939.3:c.3237A>C	NP_008870.2:p.Thr1079=
NM_006939.4:c.3237A>C MANE Select	NP_008870.2:p.Thr1079=