LDH info

Canonical Allele Identifier: CA13649949
Gene: TPH2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10879357

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020783A>G , CM000674.2:g.72020783A>G GRCh38
NC_000012.11:g.72414563A>G , CM000674.1:g.72414563A>G GRCh37
NC_000012.10:g.70700830A>G NCBI36
NG_008279.1:g.86938A>G

Transcript Alleles

HGVS Amino-acid change
NM_173353.3:c.1069-1616A>G VV NP_775489.2:p.=
XM_011537899.1:c.475-1616A>G XP_011536201.1:p.=
NM_173353.4:c.1069-1616A>G VV MANE Preferred NP_775489.2:p.=
ENST00000333850.3:c.1069-1616A>G ENSP00000329093.3:p.=