Canonical Allele Identifier: CA2045533091
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994522C= , CM000674.2:g.71994522C= GRCh38
NC_000012.11:g.72388302C= , CM000674.1:g.72388302C= GRCh37
NC_000012.10:g.70674569C= NCBI36
NG_008279.1:g.60677C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1025C= MANE Select ENSP00000329093.3:p.Ala342=
ENST00000333850.3:c.1025C= ENSP00000329093.3:p.Ala342=
NM_173353.3:c.1025C= NP_775489.2:p.Ala342=
XM_011537899.1:c.431C= XP_011536201.1:p.Ala144=
NM_173353.4:c.1025C= MANE Select NP_775489.2:p.Ala342=