LDH info

Canonical Allele Identifier: CA10654930
Gene: AVP HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 369949
ClinVar RCV Id: RCV000408826
dbSNP Id: rs1057516192

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083168C>A , CM000682.2:g.3083168C>A GRCh38
NC_000020.10:g.3063814C>A , CM000682.1:g.3063814C>A GRCh37
NC_000020.9:g.3011814C>A NCBI36
NG_008663.1:g.6557G>T , LRG_715:g.6557G>T

Transcript Alleles

HGVS Amino-acid change
NM_000490.4:c.131G>T , LRG_715t1:c.131G>T NP_000481.2:p.Cys44Phe
XM_011529267.1:c.131G>T XP_011527569.1:p.Cys44Phe
XM_011529267.2:c.131G>T XP_011527569.1:p.Cys44Phe
ENST00000380293.3:c.131G>T ENSP00000369647.3:p.Cys44Phe