Canonical Allele Identifier: CA2619867984
Gene: TPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994413C>A , CM000674.2:g.71994413C>A GRCh38
NC_000012.11:g.72388193C>A , CM000674.1:g.72388193C>A GRCh37
NC_000012.10:g.70674460C>A NCBI36
NG_008279.1:g.60568C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.942-26C>A MANE Select ENSP00000329093.3:n.942-26C>A
ENST00000333850.3:c.942-26C>A ENSP00000329093.3:n.942-26C>A
NM_173353.3:c.942-26C>A NP_775489.2:n.942-26C>A
XM_011537899.1:c.348-26C>A XP_011536201.1:n.348-26C>A
NM_173353.4:c.942-26C>A MANE Select NP_775489.2:n.942-26C>A