LDH info

Canonical Allele Identifier: CA114131
Gene: VWF HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 292
dbSNP Id: rs61750581

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6018581A>G , CM000674.2:g.6018581A>G GRCh38
NC_000012.11:g.6127747A>G , CM000674.1:g.6127747A>G GRCh37
NC_000012.10:g.5998008A>G NCBI36
NG_009072.1:g.111090T>C

Transcript Alleles

HGVS Amino-acid change
NM_000552.3:c.4837T>C VV NP_000543.2:p.Ser1613Pro
NM_000552.4:c.4837T>C VV NP_000543.2:p.Ser1613Pro
ENST00000261405.9:c.4837T>C ENSP00000261405.5:p.Ser1613Pro
ENST00000538635.5:n.421-24647T>C