Canonical Allele Identifier: CA2136065938
Gene: SOS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50152828G= , CM000676.2:g.50152828G= GRCh38
NC_000014.8:g.50619546G= , CM000676.1:g.50619546G= GRCh37
NC_000014.7:g.49689296G= NCBI36
NG_051073.1:g.83866C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.2161+242C= MANE Select ENSP00000216373.5:n.2161+242C=
ENST00000216373.9:c.2161+242C= ENSP00000216373.5:n.2161+242C=
ENST00000543680.5:c.2062+242C= ENSP00000445328.1:n.2062+242C=
NM_006939.2:c.2161+242C= NP_008870.2:n.2161+242C=
XM_005268021.1:c.1981+242C= XP_005268078.1:n.1981+242C=
XM_011537103.1:c.2122+242C= XP_011535405.1:n.2122+242C=
XM_011537104.1:c.2161+242C= XP_011535406.1:n.2161+242C=
NM_006939.3:c.2161+242C= NP_008870.2:n.2161+242C=
NM_006939.4:c.2161+242C= MANE Select NP_008870.2:n.2161+242C=
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