Canonical Allele Identifier: CA2045533097
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994534C= , CM000674.2:g.71994534C= GRCh38
NC_000012.11:g.72388314C= , CM000674.1:g.72388314C= GRCh37
NC_000012.10:g.70674581C= NCBI36
NG_008279.1:g.60689C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1037C= MANE Select ENSP00000329093.3:p.Ala346=
ENST00000333850.3:c.1037C= ENSP00000329093.3:p.Ala346=
NM_173353.3:c.1037C= NP_775489.2:p.Ala346=
XM_011537899.1:c.443C= XP_011536201.1:p.Ala148=
NM_173353.4:c.1037C= MANE Select NP_775489.2:p.Ala346=