LDH info

Canonical Allele Identifier: CA127503
Gene: APOE HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 17852
ClinVar RCV Id: RCV000019433
dbSNP Id: rs397514253

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908531A>G , CM000681.2:g.44908531A>G GRCh38
NC_000019.9:g.45411788A>G , CM000681.1:g.45411788A>G GRCh37
NC_000019.8:g.50103628A>G NCBI36
NG_007084.2:g.7750A>G

Transcript Alleles

HGVS Amino-acid change
NM_000041.3:c.237-2A>G VV NP_000032.1:p.=
NM_001302688.1:c.315-2A>G VV NP_001289617.1:p.=
NM_001302689.1:c.237-2A>G VV NP_001289618.1:p.=
NM_001302690.1:c.237-2A>G VV NP_001289619.1:p.=
NM_001302691.1:c.237-2A>G VV NP_001289620.1:p.=
NM_000041.4:c.237-2A>G VV MANE Preferred NP_000032.1:p.=
NM_001302688.2:c.315-2A>G VV NP_001289617.1:p.=
NM_001302689.2:c.237-2A>G VV NP_001289618.1:p.=
NM_001302691.2:c.237-2A>G VV NP_001289620.1:p.=
ENST00000252486.8:c.237-2A>G ENSP00000252486.3:p.=
ENST00000425718.1:c.237-2A>G ENSP00000410423.1:p.=
ENST00000434152.5:c.315-2A>G ENSP00000413653.2:p.=
ENST00000446996.5:c.237-2A>G ENSP00000413135.1:p.=