LDH info

Canonical Allele Identifier: CA10576172
Gene: HTR2A HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 226025
dbSNP Id: rs7997012

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46837850A>G , CM000675.2:g.46837850A>G GRCh38
NC_000013.10:g.47411985A>G , CM000675.1:g.47411985A>G GRCh37
NC_000013.9:g.46309986A>G NCBI36
NG_013011.1:g.64185T>C

Transcript Alleles

HGVS Amino-acid change
NM_000621.4:c.614-2211T>C VV NP_000612.1:p.=
NM_001165947.2:c.362-2211T>C VV NP_001159419.1:p.=
ENST00000378688.8:c.614-2211T>C ENSP00000367959.3:p.=
ENST00000542664.3:c.614-2211T>C ENSP00000437737.1:p.=
ENST00000543956.4:c.362-2211T>C ENSP00000441861.1:p.=