Canonical Allele Identifier: CA2509437004
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71943078G>T , CM000674.2:g.71943078G>T GRCh38
NC_000012.11:g.72336858G>T , CM000674.1:g.72336858G>T GRCh37
NC_000012.10:g.70623125G>T NCBI36
NG_008279.1:g.9233G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.256-1216G>T MANE Select ENSP00000329093.3:n.256-1216G>T
ENST00000333850.3:c.256-1216G>T ENSP00000329093.3:n.256-1216G>T
ENST00000546576.1:n.266-1216G>T
NM_173353.3:c.256-1216G>T NP_775489.2:n.256-1216G>T
XR_245894.2:n.356-1216G>T
XR_001748575.1:n.356-1216G>T
NM_173353.4:c.256-1216G>T MANE Select NP_775489.2:n.256-1216G>T