Canonical Allele Identifier: CA2136065998

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50152949A= , CM000676.2:g.50152949A=	GRCh38
NC_000014.8:g.50619667A= , CM000676.1:g.50619667A=	GRCh37
NC_000014.7:g.49689417A=	NCBI36
NG_051073.1:g.83745T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.2161+121T= MANE Select	ENSP00000216373.5:n.2161+121T=
ENST00000216373.9:c.2161+121T=	ENSP00000216373.5:n.2161+121T=
ENST00000543680.5:c.2062+121T=	ENSP00000445328.1:n.2062+121T=
NM_006939.2:c.2161+121T=	NP_008870.2:n.2161+121T=
XM_005268021.1:c.1981+121T=	XP_005268078.1:n.1981+121T=
XM_011537103.1:c.2122+121T=	XP_011535405.1:n.2122+121T=
XM_011537104.1:c.2161+121T=	XP_011535406.1:n.2161+121T=
NM_006939.3:c.2161+121T=	NP_008870.2:n.2161+121T=
NM_006939.4:c.2161+121T= MANE Select	NP_008870.2:n.2161+121T=