Canonical Allele Identifier: CA2552744275
Gene: TPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994433dup , CM000674.2:g.71994433dup GRCh38
NC_000012.11:g.72388213dup , CM000674.1:g.72388213dup GRCh37
NC_000012.10:g.70674480dup NCBI36
NG_008279.1:g.60588dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.942-6dup MANE Select ENSP00000329093.3:n.942-6dup
ENST00000333850.3:c.942-6dup ENSP00000329093.3:n.942-6dup
NM_173353.3:c.942-6dup NP_775489.2:n.942-6dup
XM_011537899.1:c.348-6dup XP_011536201.1:n.348-6dup
NM_173353.4:c.942-6dup MANE Select NP_775489.2:n.942-6dup