Canonical Allele Identifier: CA2136065902
Gene: SOS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50152758A= , CM000676.2:g.50152758A= GRCh38
NC_000014.8:g.50619476A= , CM000676.1:g.50619476A= GRCh37
NC_000014.7:g.49689226A= NCBI36
NG_051073.1:g.83936T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.2161+312T= MANE Select ENSP00000216373.5:n.2161+312T=
ENST00000216373.9:c.2161+312T= ENSP00000216373.5:n.2161+312T=
ENST00000543680.5:c.2062+312T= ENSP00000445328.1:n.2062+312T=
NM_006939.2:c.2161+312T= NP_008870.2:n.2161+312T=
XM_005268021.1:c.1981+312T= XP_005268078.1:n.1981+312T=
XM_011537103.1:c.2122+312T= XP_011535405.1:n.2122+312T=
XM_011537104.1:c.2161+312T= XP_011535406.1:n.2161+312T=
NM_006939.3:c.2161+312T= NP_008870.2:n.2161+312T=
NM_006939.4:c.2161+312T= MANE Select NP_008870.2:n.2161+312T=
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