Canonical Allele Identifier: CA389640490
Gene: SOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130573G>T , CM000676.2:g.50130573G>T GRCh38
NC_000014.8:g.50597291G>T , CM000676.1:g.50597291G>T GRCh37
NC_000014.7:g.49667041G>T NCBI36
NG_051073.1:g.106121C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.3265C>A MANE Select ENSP00000216373.5:p.Pro1089Thr
ENST00000216373.9:c.3265C>A ENSP00000216373.5:p.Pro1089Thr
ENST00000543680.5:c.3166C>A ENSP00000445328.1:p.Pro1056Thr
NM_006939.2:c.3265C>A NP_008870.2:p.Pro1089Thr
XM_005268021.1:c.3085C>A XP_005268078.1:p.Pro1029Thr
XM_011537103.1:c.3226C>A XP_011535405.1:p.Pro1076Thr
NM_006939.3:c.3265C>A NP_008870.2:p.Pro1089Thr
NM_006939.4:c.3265C>A MANE Select NP_008870.2:p.Pro1089Thr