LDH info

Canonical Allele Identifier: CA041273
Gene: APOE HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs267606664

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908730G>A , CM000681.2:g.44908730G>A GRCh38
NC_000019.9:g.45411987G>A , CM000681.1:g.45411987G>A GRCh37
NC_000019.8:g.50103827G>A NCBI36
NG_007084.2:g.7949G>A

Transcript Alleles

HGVS Amino-acid change
NM_000041.3:c.434G>A VV NP_000032.1:p.Gly145Asp
NM_001302688.1:c.512G>A VV NP_001289617.1:p.Gly171Asp
NM_001302689.1:c.434G>A VV NP_001289618.1:p.Gly145Asp
NM_001302690.1:c.434G>A VV NP_001289619.1:p.Gly145Asp
NM_001302691.1:c.434G>A VV NP_001289620.1:p.Gly145Asp
NM_000041.4:c.434G>A VV MANE Preferred NP_000032.1:p.Gly145Asp
NM_001302688.2:c.512G>A VV NP_001289617.1:p.Gly171Asp
NM_001302689.2:c.434G>A VV NP_001289618.1:p.Gly145Asp
NM_001302691.2:c.434G>A VV NP_001289620.1:p.Gly145Asp
ENST00000252486.8:c.434G>A ENSP00000252486.3:p.Gly145Asp
ENST00000425718.1:c.434G>A ENSP00000410423.1:p.Gly145Asp
ENST00000434152.5:c.512G>A ENSP00000413653.2:p.Gly171Asp
ENST00000446996.5:c.434G>A ENSP00000413135.1:p.Gly145Asp