Canonical Allele Identifier: CA2136058847
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130603T= , CM000676.2:g.50130603T= GRCh38
NC_000014.8:g.50597321T= , CM000676.1:g.50597321T= GRCh37
NC_000014.7:g.49667071T= NCBI36
NG_051073.1:g.106091A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.3235A= MANE Select ENSP00000216373.5:p.Thr1079=
ENST00000216373.9:c.3235A= ENSP00000216373.5:p.Thr1079=
ENST00000543680.5:c.3136A= ENSP00000445328.1:p.Thr1046=
NM_006939.2:c.3235A= NP_008870.2:p.Thr1079=
XM_005268021.1:c.3055A= XP_005268078.1:p.Thr1019=
XM_011537103.1:c.3196A= XP_011535405.1:p.Thr1066=
NM_006939.3:c.3235A= NP_008870.2:p.Thr1079=
NM_006939.4:c.3235A= MANE Select NP_008870.2:p.Thr1079=