Canonical Allele Identifier: CA2136066043
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50153039T= , CM000676.2:g.50153039T= GRCh38
NC_000014.8:g.50619757T= , CM000676.1:g.50619757T= GRCh37
NC_000014.7:g.49689507T= NCBI36
NG_051073.1:g.83655A=

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.2161+31A= MANE Select ENSP00000216373.5:n.2161+31A=
ENST00000216373.9:c.2161+31A= ENSP00000216373.5:n.2161+31A=
ENST00000543680.5:c.2062+31A= ENSP00000445328.1:n.2062+31A=
NM_006939.2:c.2161+31A= NP_008870.2:n.2161+31A=
XM_005268021.1:c.1981+31A= XP_005268078.1:n.1981+31A=
XM_011537103.1:c.2122+31A= XP_011535405.1:n.2122+31A=
XM_011537104.1:c.2161+31A= XP_011535406.1:n.2161+31A=
NM_006939.3:c.2161+31A= NP_008870.2:n.2161+31A=
NM_006939.4:c.2161+31A= MANE Select NP_008870.2:n.2161+31A=