Canonical Allele Identifier: CA2575227521
Gene: TPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938954del , CM000674.2:g.71938954del GRCh38
NC_000012.11:g.72332734del , CM000674.1:g.72332734del GRCh37
NC_000012.10:g.70619001del NCBI36
NG_008279.1:g.5109del

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-33del MANE Select ENSP00000329093.3:n.-33del
ENST00000333850.3:c.-33del ENSP00000329093.3:n.-33del
NM_173353.3:c.-33del NP_775489.2:n.-33del
XR_245894.2:n.68del
XR_001748575.1:n.68del
NM_173353.4:c.-33del MANE Select NP_775489.2:n.-33del