Canonical Allele Identifier: CA389647673

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50649219G>T (hg19) ; chr14:g.50182501G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50182501G>T , CM000676.2:g.50182501G>T	GRCh38
NC_000014.8:g.50649219G>T , CM000676.1:g.50649219G>T	GRCh37
NC_000014.7:g.49718969G>T	NCBI36
NG_051073.1:g.54193C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.820C>A MANE Select	ENSP00000216373.5:p.His274Asn
ENST00000216373.9:c.820C>A	ENSP00000216373.5:p.His274Asn
ENST00000543680.5:c.820C>A	ENSP00000445328.1:p.His274Asn
ENST00000556469.5:n.587C>A
NM_006939.2:c.820C>A	NP_008870.2:p.His274Asn
XM_005268021.1:c.640C>A	XP_005268078.1:p.His214Asn
XM_011537103.1:c.781C>A	XP_011535405.1:p.His261Asn
XM_011537104.1:c.820C>A	XP_011535406.1:p.His274Asn
XR_943842.1:n.954-1286G>T
XR_943843.1:n.954-1286G>T
NM_006939.3:c.820C>A	NP_008870.2:p.His274Asn
NM_006939.4:c.820C>A MANE Select	NP_008870.2:p.His274Asn