LDH info

Canonical Allele Identifier: CA120698
Gene: AR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9811
ClinVar RCV Id: RCV000010485
dbSNP Id: rs137852568

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67723728A>T , CM000685.2:g.67723728A>T GRCh38
NC_000023.10:g.66943570A>T , CM000685.1:g.66943570A>T GRCh37
NC_000023.9:g.66860295A>T NCBI36
NG_009014.2:g.184697A>T

Transcript Alleles

HGVS Amino-acid change
NM_000044.3:c.2650A>T VV NP_000035.2:p.Lys884Ter
NM_001011645.2:c.1054A>T VV NP_001011645.1:p.Lys352Ter
NM_000044.4:c.2650A>T VV NP_000035.2:p.Lys884Ter
NM_001011645.3:c.1054A>T VV NP_001011645.1:p.Lys352Ter
ENST00000374690.7:c.2650A>T ENSP00000363822.3:p.Lys884Ter
ENST00000396043.2:c.1054A>T ENSP00000379358.2:p.Lys352Ter
ENST00000396044.7:c.*11A>T ENSP00000379359.3:p.=
ENST00000612452.4:c.2101A>T ENSP00000484033.1:p.Lys701Ter