LDH info

Canonical Allele Identifier: CA130214
Gene: GNRHR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16036
ClinVar RCV Id: RCV000030920
dbSNP Id: rs104893847

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740508G>A , CM000666.2:g.67740508G>A GRCh38
NC_000004.11:g.68606226G>A , CM000666.1:g.68606226G>A GRCh37
NC_000004.10:g.68288821G>A NCBI36
NG_009293.1:g.20579C>T

Transcript Alleles

HGVS Amino-acid change
NM_000406.2:c.959C>T VV NP_000397.1:p.Pro320Leu
NM_001012763.1:c.*81C>T VV NP_001012781.1:p.=
ENST00000226413.4:c.959C>T ENSP00000226413.4:p.Pro320Leu
ENST00000420975.2:n.831C>T ENSP00000397561.2:p.=