LDH info

Canonical Allele Identifier: CA331889
Gene: RAD50 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 128024
dbSNP Id: rs377260382

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132557327G>A , CM000667.2:g.132557327G>A GRCh38
NC_000005.9:g.131893019G>A , CM000667.1:g.131893019G>A GRCh37
NC_000005.8:g.131920918G>A NCBI36
NG_021151.1:g.5404G>A
NG_021151.2:g.5351G>A

Transcript Alleles

HGVS Amino-acid change
NM_005732.3:c.3G>A VV
NM_005732.4:c.3G>A VV MANE Preferred
ENST00000378823.7:c.3G>A
ENST00000416135.5:c.-169+854G>A ENSP00000389515.1:p.=
ENST00000423956.5:c.3G>A
ENST00000453394.5:c.3G>A
ENST00000533482.5:c.3G>A