Canonical Allele Identifier: CA2045533100
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994540A= , CM000674.2:g.71994540A= GRCh38
NC_000012.11:g.72388320A= , CM000674.1:g.72388320A= GRCh37
NC_000012.10:g.70674587A= NCBI36
NG_008279.1:g.60695A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1043A= MANE Select ENSP00000329093.3:p.Asp348=
ENST00000333850.3:c.1043A= ENSP00000329093.3:p.Asp348=
NM_173353.3:c.1043A= NP_775489.2:p.Asp348=
XM_011537899.1:c.449A= XP_011536201.1:p.Asp150=
NM_173353.4:c.1043A= MANE Select NP_775489.2:p.Asp348=