Canonical Allele Identifier: CA605810976
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1458783597

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938951C>T , CM000674.2:g.71938951C>T GRCh38
NC_000012.11:g.72332731C>T , CM000674.1:g.72332731C>T GRCh37
NC_000012.10:g.70618998C>T NCBI36
NG_008279.1:g.5106C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-36C>T MANE Select ENSP00000329093.3:n.-36C>T
ENST00000333850.3:c.-36C>T ENSP00000329093.3:n.-36C>T
NM_173353.3:c.-36C>T NP_775489.2:n.-36C>T
XR_245894.2:n.65C>T
XR_001748575.1:n.65C>T
NM_173353.4:c.-36C>T MANE Select NP_775489.2:n.-36C>T