LDH info

Canonical Allele Identifier: CA256770
Gene: POMC HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13355
ClinVar RCV Id: RCV000014283
dbSNP Id: rs753856820

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25164783G>T , CM000664.2:g.25164783G>T GRCh38
NC_000002.11:g.25387652G>T , CM000664.1:g.25387652G>T GRCh37
NC_000002.10:g.25241156G>T NCBI36
NG_008997.1:g.8908C>A

Transcript Alleles

HGVS Amino-acid change
NM_000939.2:c.-11C>A VV NP_000930.1:p.=
NM_001035256.1:c.-11C>A VV NP_001030333.1:p.=
XM_011532917.1:c.-11C>A XP_011531219.1:p.=
NM_000939.3:c.-11C>A VV NP_000930.1:p.=
NM_001035256.2:c.-11C>A VV NP_001030333.1:p.=
NM_001319204.1:c.-11C>A VV NP_001306133.1:p.=
NM_001319205.1:c.-11C>A VV NP_001306134.1:p.=
NM_000939.4:c.-11C>A VV MANE Preferred NP_000930.1:p.=
ENST00000264708.7:c.-11C>A ENSP00000264708.3:p.=
ENST00000380794.5:c.-11C>A ENSP00000370171.1:p.=
ENST00000395826.6:c.-11C>A ENSP00000379170.2:p.=
ENST00000405623.5:c.-11C>A ENSP00000384092.1:p.=
ENST00000449220.1:c.-11C>A ENSP00000387993.1:p.=