LDH info

Canonical Allele Identifier: CA116116
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 3258
dbSNP Id: rs104894658

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885298C>A , CM000680.2:g.13885298C>A GRCh38
NC_000018.9:g.13885297C>A , CM000680.1:g.13885297C>A GRCh37
NC_000018.8:g.13875297C>A NCBI36
NG_011819.1:g.35239G>T

Transcript Alleles

HGVS Amino-acid change
NM_000529.2:c.221G>T VV NP_000520.1:p.Ser74Ile
NM_001291911.1:c.221G>T VV NP_001278840.1:p.Ser74Ile
XM_017025781.1:c.221G>T XP_016881270.1:p.Ser74Ile
ENST00000327606.3:c.221G>T ENSP00000333821.2:p.Ser74Ile
ENST00000399821.2:c.221G>T ENSP00000382718.2:p.Ser74Ile