LDH info

Canonical Allele Identifier: CA14378452
Gene: ORMDL3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12603332

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39926554T>C , CM000679.2:g.39926554T>C GRCh38
NC_000017.10:g.38082807T>C , CM000679.1:g.38082807T>C GRCh37
NC_000017.9:g.35336333T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_139280.2:c.-23+930A>G VV NP_644809.1:p.=
XM_005257825.3:c.-23+263A>G XP_005257882.2:p.=
XM_005257827.2:c.-18+930A>G XP_005257884.1:p.=
NM_001320801.1:c.-1208A>G VV NP_001307730.1:p.=
NM_001320802.1:c.-18+930A>G VV NP_001307731.1:p.=
NM_001320803.1:c.-23+263A>G VV NP_001307732.1:p.=
NM_139280.3:c.-23+930A>G VV NP_644809.1:p.=
NM_139280.4:c.-23+930A>G VV MANE Preferred NP_644809.1:p.=
NM_001320802.2:c.-18+930A>G VV NP_001307731.1:p.=
ENST00000304046.6:c.-23+930A>G ENSP00000304858.2:p.=
ENST00000394169.5:c.-1208A>G ENSP00000377724.1:p.=
ENST00000579695.5:c.-18+930A>G ENSP00000464693.1:p.=
ENST00000582052.1:n.31-215A>G
ENST00000584000.1:c.-23+513A>G ENSP00000464298.1:p.=