Canonical Allele Identifier: CA2045533128
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994615G= , CM000674.2:g.71994615G= GRCh38
NC_000012.11:g.72388395G= , CM000674.1:g.72388395G= GRCh37
NC_000012.10:g.70674662G= NCBI36
NG_008279.1:g.60770G=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1068+50G= MANE Select ENSP00000329093.3:n.1068+50G=
ENST00000333850.3:c.1068+50G= ENSP00000329093.3:n.1068+50G=
NM_173353.3:c.1068+50G= NP_775489.2:n.1068+50G=
XM_011537899.1:c.474+50G= XP_011536201.1:n.474+50G=
NM_173353.4:c.1068+50G= MANE Select NP_775489.2:n.1068+50G=