LDH info

Canonical Allele Identifier: CA12203829
Gene: FOXO3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2802292

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108587315G>T , CM000668.2:g.108587315G>T GRCh38
NC_000006.11:g.108908518G>T , CM000668.1:g.108908518G>T GRCh37
NC_000006.10:g.109015211G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001455.3:c.621+25486G>T VV NP_001446.1:p.=
NM_201559.2:c.621+25486G>T VV NP_963853.1:p.=
XM_005266867.3:c.-64+25486G>T XP_005266924.1:p.=
XM_011535626.1:c.120+25172G>T XP_011533928.1:p.=
XM_011535627.1:c.69+679G>T XP_011533929.1:p.=
XM_005266867.4:c.-64+25486G>T XP_005266924.1:p.=
XM_011535626.2:c.120+25172G>T XP_011533928.1:p.=
XM_011535628.3:c.-2540G>T XP_011533930.1:p.=
XM_017010585.1:c.-64+17573G>T XP_016866074.1:p.=
XM_017010586.1:c.-40+17573G>T XP_016866075.1:p.=
NM_001455.4:c.621+25486G>T VV MANE Preferred NP_001446.1:p.=
ENST00000343882.10:c.621+25486G>T ENSP00000339527.6:p.=
ENST00000406360.1:c.621+25486G>T ENSP00000385824.1:p.=