LDH info

Canonical Allele Identifier: CA121961
Gene: AVP HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 12213
ClinVar RCV Id: RCV000012997
dbSNP Id: rs121964887

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083138C>A , CM000682.2:g.3083138C>A GRCh38
NC_000020.10:g.3063784C>A , CM000682.1:g.3063784C>A GRCh37
NC_000020.9:g.3011784C>A NCBI36
NG_008663.1:g.6587G>T , LRG_715:g.6587G>T

Transcript Alleles

HGVS Amino-acid change
NM_000490.4:c.161G>T , LRG_715t1:c.161G>T NP_000481.2:p.Gly54Val
XM_011529267.1:c.161G>T XP_011527569.1:p.Gly54Val
XM_011529267.2:c.161G>T XP_011527569.1:p.Gly54Val
NM_000490.5:c.161G>T VV MANE Preferred NP_000481.2:p.Gly54Val
ENST00000380293.3:c.161G>T ENSP00000369647.3:p.Gly54Val