LDH info

Canonical Allele Identifier: CA130197
Gene: GNRHR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16023
dbSNP Id: rs104893836

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754019T>C , CM000666.2:g.67754019T>C GRCh38
NC_000004.11:g.68619737T>C , CM000666.1:g.68619737T>C GRCh37
NC_000004.10:g.68302332T>C NCBI36
NG_009293.1:g.7068A>G

Transcript Alleles

HGVS Amino-acid change
NM_000406.2:c.317A>G VV NP_000397.1:p.Gln106Arg
NM_001012763.1:c.317A>G VV NP_001012781.1:p.Gln106Arg
ENST00000226413.4:c.317A>G ENSP00000226413.4:p.Gln106Arg
ENST00000420975.2:n.317A>G ENSP00000397561.2:p.Gln106Arg