LDH info

Canonical Allele Identifier: CA127502
Gene: APOE HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 17851
dbSNP Id: rs769455

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908783C>T , CM000681.2:g.44908783C>T GRCh38
NC_000019.9:g.45412040C>T , CM000681.1:g.45412040C>T GRCh37
NC_000019.8:g.50103880C>T NCBI36
NG_007084.2:g.8002C>T

Transcript Alleles

HGVS Amino-acid change
NM_000041.3:c.487C>T VV NP_000032.1:p.Arg163Cys
NM_001302688.1:c.565C>T VV NP_001289617.1:p.Arg189Cys
NM_001302689.1:c.487C>T VV NP_001289618.1:p.Arg163Cys
NM_001302690.1:c.487C>T VV NP_001289619.1:p.Arg163Cys
NM_001302691.1:c.487C>T VV NP_001289620.1:p.Arg163Cys
NM_000041.4:c.487C>T VV MANE Preferred NP_000032.1:p.Arg163Cys
NM_001302688.2:c.565C>T VV NP_001289617.1:p.Arg189Cys
NM_001302689.2:c.487C>T VV NP_001289618.1:p.Arg163Cys
NM_001302691.2:c.487C>T VV NP_001289620.1:p.Arg163Cys
ENST00000252486.8:c.487C>T ENSP00000252486.3:p.Arg163Cys
ENST00000425718.1:c.487C>T ENSP00000410423.1:p.Arg163Cys
ENST00000434152.5:c.565C>T ENSP00000413653.2:p.Arg189Cys
ENST00000446996.5:c.487C>T ENSP00000413135.1:p.Arg163Cys