Canonical Allele Identifier: CA2619886912
Gene: TPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938979C>T , CM000674.2:g.71938979C>T GRCh38
NC_000012.11:g.72332759C>T , CM000674.1:g.72332759C>T GRCh37
NC_000012.10:g.70619026C>T NCBI36
NG_008279.1:g.5134C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-8C>T MANE Select ENSP00000329093.3:n.-8C>T
ENST00000333850.3:c.-8C>T ENSP00000329093.3:n.-8C>T
ENST00000546576.1:n.3C>T
NM_173353.3:c.-8C>T NP_775489.2:n.-8C>T
XR_245894.2:n.93C>T
XR_001748575.1:n.93C>T
NM_173353.4:c.-8C>T MANE Select NP_775489.2:n.-8C>T