LDH info

Canonical Allele Identifier: CA11094208
Gene: HSPD1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs788016

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197487569G>A , CM000664.2:g.197487569G>A GRCh38
NC_000002.11:g.198352293G>A , CM000664.1:g.198352293G>A GRCh37
NC_000002.10:g.198060538G>A NCBI36
NG_008915.1:g.17706C>T

Transcript Alleles

HGVS Amino-acid change
NM_002156.4:c.1569+289C>T VV NP_002147.2:p.=
NM_199440.1:c.1569+289C>T VV NP_955472.1:p.=
XM_005246518.2:c.1569+289C>T XP_005246575.1:p.=
NM_002156.5:c.1569+289C>T VV MANE Preferred NP_002147.2:p.=
ENST00000345042.6:c.1569+289C>T ENSP00000340019.2:p.=
ENST00000388968.7:c.1569+289C>T ENSP00000373620.3:p.=