LDH info

Canonical Allele Identifier: CA120777
Gene: AR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9847
ClinVar RCV Id: RCV000010521
dbSNP Id: rs137852592

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67721937T>C , CM000685.2:g.67721937T>C GRCh38
NC_000023.10:g.66941779T>C , CM000685.1:g.66941779T>C GRCh37
NC_000023.9:g.66858504T>C NCBI36
NG_009014.2:g.182906T>C

Transcript Alleles

HGVS Amino-acid change
NM_000044.3:c.2423T>C VV NP_000035.2:p.Met808Thr
NM_001011645.2:c.827T>C VV NP_001011645.1:p.Met276Thr
NM_000044.4:c.2423T>C VV NP_000035.2:p.Met808Thr
NM_001011645.3:c.827T>C VV NP_001011645.1:p.Met276Thr
NM_000044.6:c.2423T>C VV MANE Preferred NP_000035.2:p.Met808Thr
ENST00000374690.7:c.2423T>C ENSP00000363822.3:p.Met808Thr
ENST00000396043.2:c.827T>C ENSP00000379358.2:p.Met276Thr
ENST00000396044.7:c.2174-1749T>C ENSP00000379359.3:p.=
ENST00000612452.4:c.1853T>C ENSP00000484033.1:p.Met618Thr