Canonical Allele Identifier: CA385782051
Gene: TPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994513T>C , CM000674.2:g.71994513T>C GRCh38
NC_000012.11:g.72388293T>C , CM000674.1:g.72388293T>C GRCh37
NC_000012.10:g.70674560T>C NCBI36
NG_008279.1:g.60668T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1016T>C MANE Select ENSP00000329093.3:p.Ile339Thr
ENST00000333850.3:c.1016T>C ENSP00000329093.3:p.Ile339Thr
NM_173353.3:c.1016T>C NP_775489.2:p.Ile339Thr
XM_011537899.1:c.422T>C XP_011536201.1:p.Ile141Thr
NM_173353.4:c.1016T>C MANE Select NP_775489.2:p.Ile339Thr