Canonical Allele Identifier: CA480773853
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs120074176
MyVariant Identifiers: chr12:g.72372833C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71979053C>A , CM000674.2:g.71979053C>A GRCh38
NC_000012.11:g.72372833C>A , CM000674.1:g.72372833C>A GRCh37
NC_000012.10:g.70659100C>A NCBI36
NG_008279.1:g.45208C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.907C>A MANE Select ENSP00000329093.3:p.Arg303=
ENST00000333850.3:c.907C>A ENSP00000329093.3:p.Arg303=
NM_173353.3:c.907C>A NP_775489.2:p.Arg303=
XM_011537899.1:c.313C>A XP_011536201.1:p.Arg105=
NM_173353.4:c.907C>A MANE Select NP_775489.2:p.Arg303=