LDH info

Canonical Allele Identifier: CA116121
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 3262
ClinVar RCV Id: RCV000003418
dbSNP Id: rs104894661

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885200C>T , CM000680.2:g.13885200C>T GRCh38
NC_000018.9:g.13885199C>T , CM000680.1:g.13885199C>T GRCh37
NC_000018.8:g.13875199C>T NCBI36
NG_011819.1:g.35337G>A

Transcript Alleles

HGVS Amino-acid change
NM_000529.2:c.319G>A VV NP_000520.1:p.Asp107Asn
NM_001291911.1:c.319G>A VV NP_001278840.1:p.Asp107Asn
XM_017025781.1:c.319G>A XP_016881270.1:p.Asp107Asn
ENST00000327606.3:c.319G>A ENSP00000333821.2:p.Asp107Asn
ENST00000399821.2:c.319G>A ENSP00000382718.2:p.Asp107Asn