Canonical Allele Identifier: CA389649660

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50666509A>G (hg19) ; chr14:g.50199791A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199791A>G , CM000676.2:g.50199791A>G	GRCh38
NC_000014.8:g.50666509A>G , CM000676.1:g.50666509A>G	GRCh37
NC_000014.7:g.49736259A>G	NCBI36
NG_051073.1:g.36903T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.410T>C MANE Select	ENSP00000216373.5:p.Ile137Thr
ENST00000216373.9:c.410T>C	ENSP00000216373.5:p.Ile137Thr
ENST00000543680.5:c.410T>C	ENSP00000445328.1:p.Ile137Thr
ENST00000555666.1:n.589T>C
ENST00000556469.5:n.381T>C
NM_006939.2:c.410T>C	NP_008870.2:p.Ile137Thr
XM_005268021.1:c.230T>C	XP_005268078.1:p.Ile77Thr
XM_011537103.1:c.371T>C	XP_011535405.1:p.Ile124Thr
XM_011537104.1:c.410T>C	XP_011535406.1:p.Ile137Thr
XR_943842.1:n.1039+15919A>G
XR_943843.1:n.1039+15919A>G
NM_006939.3:c.410T>C	NP_008870.2:p.Ile137Thr
NM_006939.4:c.410T>C MANE Select	NP_008870.2:p.Ile137Thr