LDH info

Canonical Allele Identifier: CA5217784
Gene: C5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 402454
ClinVar RCV Id: RCV000454843
dbSNP Id: rs17611

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.121006922C>T , CM000671.2:g.121006922C>T GRCh38
NC_000009.11:g.123769200C>T , CM000671.1:g.123769200C>T GRCh37
NC_000009.10:g.122809021C>T NCBI36
NG_007364.1:g.48355G>A , LRG_28:g.48355G>A

Transcript Alleles

HGVS Amino-acid change
NM_001735.2:c.2404G>A , LRG_28t1:c.2404G>A NP_001726.2:p.Val802Ile
XM_011518980.1:c.2419G>A XP_011517282.1:p.Val807Ile
XM_011518981.1:c.2422G>A XP_011517283.1:p.Val808Ile
NM_001317163.1:c.2422G>A VV NP_001304092.1:p.Val808Ile
NM_001317164.1:c.2404G>A VV NP_001304093.1:p.Val802Ile
ENST00000223642.2:c.2404G>A ENSP00000223642.1:p.Val802Ile
ENST00000466280.1:n.7G>A