Canonical Allele Identifier: CA2136066038

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50153028C= , CM000676.2:g.50153028C=	GRCh38
NC_000014.8:g.50619746C= , CM000676.1:g.50619746C=	GRCh37
NC_000014.7:g.49689496C=	NCBI36
NG_051073.1:g.83666G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+42G= MANE Select	ENSP00000216373.5:n.2161+42G=
ENST00000216373.9:c.2161+42G=	ENSP00000216373.5:n.2161+42G=
ENST00000543680.5:c.2062+42G=	ENSP00000445328.1:n.2062+42G=
NM_006939.2:c.2161+42G=	NP_008870.2:n.2161+42G=
XM_005268021.1:c.1981+42G=	XP_005268078.1:n.1981+42G=
XM_011537103.1:c.2122+42G=	XP_011535405.1:n.2122+42G=
XM_011537104.1:c.2161+42G=	XP_011535406.1:n.2161+42G=
NM_006939.3:c.2161+42G=	NP_008870.2:n.2161+42G=
NM_006939.4:c.2161+42G= MANE Select	NP_008870.2:n.2161+42G=