Canonical Allele Identifier: CA2045533086
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994511A= , CM000674.2:g.71994511A= GRCh38
NC_000012.11:g.72388291A= , CM000674.1:g.72388291A= GRCh37
NC_000012.10:g.70674558A= NCBI36
NG_008279.1:g.60666A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1014A= MANE Select ENSP00000329093.3:p.Glu338=
ENST00000333850.3:c.1014A= ENSP00000329093.3:p.Glu338=
NM_173353.3:c.1014A= NP_775489.2:p.Glu338=
XM_011537899.1:c.420A= XP_011536201.1:p.Glu140=
NM_173353.4:c.1014A= MANE Select NP_775489.2:p.Glu338=