Canonical Allele Identifier: CA2136058793

Gene: SOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130499A= , CM000676.2:g.50130499A=	GRCh38
NC_000014.8:g.50597217A= , CM000676.1:g.50597217A=	GRCh37
NC_000014.7:g.49666967A=	NCBI36
NG_051073.1:g.106195T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216373.10:c.3337+2T= MANE Select	ENSP00000216373.5:n.3337+2T=
ENST00000216373.9:c.3337+2T=	ENSP00000216373.5:n.3337+2T=
ENST00000543680.5:c.3238+2T=	ENSP00000445328.1:n.3238+2T=
NM_006939.2:c.3337+2T=	NP_008870.2:n.3337+2T=
XM_005268021.1:c.3157+2T=	XP_005268078.1:n.3157+2T=
XM_011537103.1:c.3298+2T=	XP_011535405.1:n.3298+2T=
NM_006939.3:c.3337+2T=	NP_008870.2:n.3337+2T=
NM_006939.4:c.3337+2T= MANE Select	NP_008870.2:n.3337+2T=