Canonical Allele Identifier: CA2045533050
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994416C= , CM000674.2:g.71994416C= GRCh38
NC_000012.11:g.72388196C= , CM000674.1:g.72388196C= GRCh37
NC_000012.10:g.70674463C= NCBI36
NG_008279.1:g.60571C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.942-23C= MANE Select ENSP00000329093.3:n.942-23C=
ENST00000333850.3:c.942-23C= ENSP00000329093.3:n.942-23C=
NM_173353.3:c.942-23C= NP_775489.2:n.942-23C=
XM_011537899.1:c.348-23C= XP_011536201.1:n.348-23C=
NM_173353.4:c.942-23C= MANE Select NP_775489.2:n.942-23C=