LDH info

Canonical Allele Identifier: CA99073617
Gene: GC HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs222029

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71779245G>A , CM000666.2:g.71779245G>A GRCh38
NC_000004.11:g.72644962G>A , CM000666.1:g.72644962G>A GRCh37
NC_000004.10:g.72863826G>A NCBI36
NG_012837.2:g.31276C>T
NG_012837.3:g.31276C>T

Transcript Alleles

HGVS Amino-acid change
NM_000583.3:c.58+4716C>T VV NP_000574.2:p.=
NM_001204306.1:c.58+4716C>T VV NP_001191235.1:p.=
NM_001204307.1:c.115+4716C>T VV NP_001191236.1:p.=
XM_006714177.2:c.58+4716C>T XP_006714240.1:p.=
XM_006714177.3:c.58+4716C>T XP_006714240.1:p.=
NM_000583.4:c.58+4716C>T VV MANE Preferred NP_000574.2:p.=
ENST00000273951.12:c.58+4716C>T ENSP00000273951.8:p.=
ENST00000504199.5:c.115+4716C>T ENSP00000421725.1:p.=
ENST00000506245.1:c.58+4716C>T ENSP00000426718.1:p.=
ENST00000509740.5:c.58+4716C>T ENSP00000422664.1:p.=
ENST00000513476.5:c.58+4716C>T ENSP00000426683.1:p.=