Canonical Allele Identifier: CA691624694
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1261526092

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71942870G>C , CM000674.2:g.71942870G>C GRCh38
NC_000012.11:g.72336650G>C , CM000674.1:g.72336650G>C GRCh37
NC_000012.10:g.70622917G>C NCBI36
NG_008279.1:g.9025G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.255+1137G>C MANE Select ENSP00000329093.3:n.255+1137G>C
ENST00000333850.3:c.255+1137G>C ENSP00000329093.3:n.255+1137G>C
ENST00000546576.1:n.265+1137G>C
NM_173353.3:c.255+1137G>C NP_775489.2:n.255+1137G>C
XR_245894.2:n.355+1137G>C
XR_001748575.1:n.355+1137G>C
NM_173353.4:c.255+1137G>C MANE Select NP_775489.2:n.255+1137G>C