Canonical Allele Identifier: CA2801534042
Gene: SOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50152705A>T , CM000676.2:g.50152705A>T GRCh38
NC_000014.8:g.50619423A>T , CM000676.1:g.50619423A>T GRCh37
NC_000014.7:g.49689173A>T NCBI36
NG_051073.1:g.83989T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.2161+365T>A MANE Select ENSP00000216373.5:n.2161+365T>A
ENST00000216373.9:c.2161+365T>A ENSP00000216373.5:n.2161+365T>A
ENST00000543680.5:c.2062+365T>A ENSP00000445328.1:n.2062+365T>A
NM_006939.2:c.2161+365T>A NP_008870.2:n.2161+365T>A
XM_005268021.1:c.1981+365T>A XP_005268078.1:n.1981+365T>A
XM_011537103.1:c.2122+365T>A XP_011535405.1:n.2122+365T>A
XM_011537104.1:c.2161+365T>A XP_011535406.1:n.2161+365T>A
NM_006939.3:c.2161+365T>A NP_008870.2:n.2161+365T>A
NM_006939.4:c.2161+365T>A MANE Select NP_008870.2:n.2161+365T>A