LDH info

Canonical Allele Identifier: CA114137
Gene: VWF HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 295
dbSNP Id: rs121964894

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6036488G>A , CM000674.2:g.6036488G>A GRCh38
NC_000012.11:g.6145654G>A , CM000674.1:g.6145654G>A GRCh37
NC_000012.10:g.6015915G>A NCBI36
NG_009072.1:g.93183C>T

Transcript Alleles

HGVS Amino-acid change
NM_000552.3:c.2446C>T VV NP_000543.2:p.Arg816Trp
NM_000552.4:c.2446C>T VV NP_000543.2:p.Arg816Trp
ENST00000261405.9:c.2446C>T ENSP00000261405.5:p.Arg816Trp
ENST00000538635.5:n.421-42554C>T