LDH info

Canonical Allele Identifier: CA342403
Gene: GNPTG HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 21714
ClinVar RCV Id: RCV000020917
dbSNP Id: rs193302847

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362037G>C , CM000678.2:g.1362037G>C GRCh38
NC_000016.9:g.1412038G>C , CM000678.1:g.1412038G>C GRCh37
NC_000016.8:g.1352039G>C NCBI36
NG_016985.1:g.15139G>C
NG_033129.1:g.57668C>G

Transcript Alleles

HGVS Amino-acid change
NM_032520.4:c.318-1G>C VV NP_115909.1:p.=
XM_017023782.1:c.366-1G>C XP_016879271.1:p.=
XM_017023783.1:c.-43-1G>C XP_016879272.1:p.=
NM_032520.5:c.318-1G>C VV MANE Preferred NP_115909.1:p.=
ENST00000204679.8:c.318-1G>C ENSP00000204679.4:p.=
ENST00000526820.5:c.*220-1G>C ENSP00000434413.1:p.=
ENST00000527076.1:n.1334-1G>C
ENST00000527168.5:n.354-1G>C
ENST00000529110.1:n.385-1G>C
ENST00000529957.5:n.417-1G>C