LDH info

Canonical Allele Identifier: CA6288959
Gene: APOA5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 420172
ClinVar RCV Id: RCV000478434
dbSNP Id: rs147528707

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116790292G>A , CM000673.2:g.116790292G>A GRCh38
NC_000011.9:g.116661008G>A , CM000673.1:g.116661008G>A GRCh37
NC_000011.8:g.116166218G>A NCBI36
NG_015894.1:g.7129C>T

Transcript Alleles

HGVS Amino-acid change
NM_001166598.1:c.937C>T VV NP_001160070.1:p.Gln313Ter
NM_052968.4:c.937C>T VV NP_443200.2:p.Gln313Ter
ENST00000227665.8:c.937C>T ENSP00000227665.4:p.Gln313Ter
ENST00000542499.5:c.937C>T ENSP00000445002.1:p.Gln313Ter