Canonical Allele Identifier: CA2045515522
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71948412T= , CM000674.2:g.71948412T= GRCh38
NC_000012.11:g.72342192T= , CM000674.1:g.72342192T= GRCh37
NC_000012.10:g.70628459T= NCBI36
NG_008279.1:g.14567T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.541-1176T= MANE Select ENSP00000329093.3:n.541-1176T=
ENST00000333850.3:c.541-1176T= ENSP00000329093.3:n.541-1176T=
ENST00000546576.1:n.551-1176T=
NM_173353.3:c.541-1176T= NP_775489.2:n.541-1176T=
XM_011537899.1:c.-55+408T= XP_011536201.1:n.-55+408T=
XR_245894.2:n.641-1176T=
XR_001748575.1:n.641-1176T=
NM_173353.4:c.541-1176T= MANE Select NP_775489.2:n.541-1176T=