LDH info

Canonical Allele Identifier: CA1209106
Gene: APOA2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 293292
ClinVar RCV Id: RCV000380848
dbSNP Id: rs6413453

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222526G>A , CM000663.2:g.161222526G>A GRCh38
NC_000001.10:g.161192316G>A , CM000663.1:g.161192316G>A GRCh37
NC_000001.9:g.159458940G>A NCBI36
NG_012043.1:g.6103C>T

Transcript Alleles

HGVS Amino-acid change
NM_001643.1:c.186-4C>T VV NP_001634.1:p.=
NM_001643.2:c.186-4C>T VV MANE Preferred NP_001634.1:p.=
ENST00000367990.7:c.186-4C>T ENSP00000356969.3:p.=
ENST00000463273.5:c.186-4C>T ENSP00000476740.1:p.=
ENST00000463812.1:c.42-4C>T ENSP00000476890.1:p.=
ENST00000464492.5:c.285-4C>T ENSP00000476911.1:p.=
ENST00000468465.5:c.42-4C>T ENSP00000476662.1:p.=
ENST00000469730.2:c.186-4C>T ENSP00000476605.1:p.=
ENST00000470459.6:c.186-4C>T ENSP00000477031.1:p.=
ENST00000481413.1:n.697-4C>T
ENST00000481511.5:c.*183-4C>T ENSP00000477054.1:p.=
ENST00000491350.1:c.53-4C>T ENSP00000477353.1:p.=