Canonical Allele Identifier: CA13593519
Gene: TPH2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4565946

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71942989C>T , CM000674.2:g.71942989C>T GRCh38
NC_000012.10:g.70623036C>T NCBI36
NC_000012.11:g.72336769C>T , CM000674.1:g.72336769C>T GRCh37
NG_008279.1:g.9144C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.3:c.255+1256C>T ENSP00000329093.3:p.=
ENST00000546576.1:n.265+1256C>T
NM_173353.3:c.255+1256C>T NP_775489.2:p.=
XR_245894.2:n.355+1256C>T