LDH info

Canonical Allele Identifier: CA239233014
Gene: TPH2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1487276

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72011279T>C , CM000674.2:g.72011279T>C GRCh38
NC_000012.11:g.72405059T>C , CM000674.1:g.72405059T>C GRCh37
NC_000012.10:g.70691326T>C NCBI36
NG_008279.1:g.77434T>C

Transcript Alleles

HGVS Amino-acid change
NM_173353.3:c.1069-11120T>C VV NP_775489.2:p.=
XM_011537899.1:c.475-11120T>C XP_011536201.1:p.=
NM_173353.4:c.1069-11120T>C VV MANE Preferred NP_775489.2:p.=
ENST00000333850.3:c.1069-11120T>C ENSP00000329093.3:p.=