LDH info

Canonical Allele Identifier: CA120737
Gene: AR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9831
ClinVar RCV Id: RCV000010505
dbSNP Id: rs137852578

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67723710A>G , CM000685.2:g.67723710A>G GRCh38
NC_000023.10:g.66943552A>G , CM000685.1:g.66943552A>G GRCh37
NC_000023.9:g.66860277A>G NCBI36
NG_009014.2:g.184679A>G

Transcript Alleles

HGVS Amino-acid change
NM_000044.3:c.2632A>G VV NP_000035.2:p.Thr878Ala
NM_001011645.2:c.1036A>G VV NP_001011645.1:p.Thr346Ala
NM_000044.4:c.2632A>G VV NP_000035.2:p.Thr878Ala
NM_001011645.3:c.1036A>G VV NP_001011645.1:p.Thr346Ala
NM_000044.6:c.2632A>G VV MANE Preferred NP_000035.2:p.Thr878Ala
ENST00000374690.7:c.2632A>G ENSP00000363822.3:p.Thr878Ala
ENST00000396043.2:c.1036A>G ENSP00000379358.2:p.Thr346Ala
ENST00000396044.7:c.2198A>G ENSP00000379359.3:p.His733Arg
ENST00000612452.4:c.2083A>G ENSP00000484033.1:p.Thr695Ala