LDH info

Canonical Allele Identifier: CA120734
Gene: AR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9830
dbSNP Id: rs137852577

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67722898C>T , CM000685.2:g.67722898C>T GRCh38
NC_000023.10:g.66942740C>T , CM000685.1:g.66942740C>T GRCh37
NC_000023.9:g.66859465C>T NCBI36
NG_009014.2:g.183867C>T

Transcript Alleles

HGVS Amino-acid change
NM_000044.3:c.2521C>T VV NP_000035.2:p.Arg841Cys
NM_001011645.2:c.925C>T VV NP_001011645.1:p.Arg309Cys
NM_000044.4:c.2521C>T VV NP_000035.2:p.Arg841Cys
NM_001011645.3:c.925C>T VV NP_001011645.1:p.Arg309Cys
NM_000044.6:c.2521C>T VV MANE Preferred NP_000035.2:p.Arg841Cys
ENST00000374690.7:c.2521C>T ENSP00000363822.3:p.Arg841Cys
ENST00000396043.2:c.925C>T ENSP00000379358.2:p.Arg309Cys
ENST00000396044.7:c.2174-788C>T ENSP00000379359.3:p.=
ENST00000612452.4:c.1972C>T ENSP00000484033.1:p.Arg658Cys