LDH info

Canonical Allele Identifier: CA022788
Gene: APOB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 128418
dbSNP Id: rs1042034

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002409C>T , CM000664.2:g.21002409C>T GRCh38
NC_000002.11:g.21225281C>T , CM000664.1:g.21225281C>T GRCh37
NC_000002.10:g.21078786C>T NCBI36
NG_011793.1:g.46665G>A

Transcript Alleles

HGVS Amino-acid change
NM_000384.2:c.13013G>A VV NP_000375.2:p.Ser4338Asn
XM_011532809.1:c.5870-3136G>A XP_011531111.1:p.=
NM_000384.3:c.13013G>A VV MANE Preferred NP_000375.3:p.Ser4338Asn
ENST00000233242.5:c.13013G>A ENSP00000233242.1:p.Ser4338Asn
ENST00000616098.4:n.13013G>A ENSP00000477990.1:p.Ser4338Asn