Canonical Allele Identifier: CA389640382
Gene: SOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130525C>G , CM000676.2:g.50130525C>G GRCh38
NC_000014.8:g.50597243C>G , CM000676.1:g.50597243C>G GRCh37
NC_000014.7:g.49666993C>G NCBI36
NG_051073.1:g.106169G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.3313G>C MANE Select ENSP00000216373.5:p.Asp1105His
ENST00000216373.9:c.3313G>C ENSP00000216373.5:p.Asp1105His
ENST00000543680.5:c.3214G>C ENSP00000445328.1:p.Asp1072His
NM_006939.2:c.3313G>C NP_008870.2:p.Asp1105His
XM_005268021.1:c.3133G>C XP_005268078.1:p.Asp1045His
XM_011537103.1:c.3274G>C XP_011535405.1:p.Asp1092His
NM_006939.3:c.3313G>C NP_008870.2:p.Asp1105His
NM_006939.4:c.3313G>C MANE Select NP_008870.2:p.Asp1105His