Canonical Allele Identifier: CA605810977
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1470133360

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938959G>T , CM000674.2:g.71938959G>T GRCh38
NC_000012.11:g.72332739G>T , CM000674.1:g.72332739G>T GRCh37
NC_000012.10:g.70619006G>T NCBI36
NG_008279.1:g.5114G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-28G>T MANE Select ENSP00000329093.3:n.-28G>T
ENST00000333850.3:c.-28G>T ENSP00000329093.3:n.-28G>T
NM_173353.3:c.-28G>T NP_775489.2:n.-28G>T
XR_245894.2:n.73G>T
XR_001748575.1:n.73G>T
NM_173353.4:c.-28G>T MANE Select NP_775489.2:n.-28G>T