LDH info

Canonical Allele Identifier: CA130206
Gene: GNRHR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16029
ClinVar RCV Id: RCV000030913
dbSNP Id: rs104893841

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740526A>T , CM000666.2:g.67740526A>T GRCh38
NC_000004.11:g.68606244A>T , CM000666.1:g.68606244A>T GRCh37
NC_000004.10:g.68288839A>T NCBI36
NG_009293.1:g.20561T>A

Transcript Alleles

HGVS Amino-acid change
NM_000406.2:c.941T>A VV NP_000397.1:p.Leu314Ter
NM_001012763.1:c.*63T>A VV NP_001012781.1:p.=
NM_000406.3:c.941T>A VV NP_000397.1:p.Leu314Ter
NM_001012763.2:c.*63T>A VV NP_001012781.1:p.=
ENST00000226413.4:c.941T>A ENSP00000226413.4:p.Leu314Ter
ENST00000420975.2:n.813T>A ENSP00000397561.2:p.=