Canonical Allele Identifier: CA2136058832
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130591G= , CM000676.2:g.50130591G= GRCh38
NC_000014.8:g.50597309G= , CM000676.1:g.50597309G= GRCh37
NC_000014.7:g.49667059G= NCBI36
NG_051073.1:g.106103C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.3247C= MANE Select ENSP00000216373.5:p.Pro1083=
ENST00000216373.9:c.3247C= ENSP00000216373.5:p.Pro1083=
ENST00000543680.5:c.3148C= ENSP00000445328.1:p.Pro1050=
NM_006939.2:c.3247C= NP_008870.2:p.Pro1083=
XM_005268021.1:c.3067C= XP_005268078.1:p.Pro1023=
XM_011537103.1:c.3208C= XP_011535405.1:p.Pro1070=
NM_006939.3:c.3247C= NP_008870.2:p.Pro1083=
NM_006939.4:c.3247C= MANE Select NP_008870.2:p.Pro1083=