Canonical Allele Identifier: CA2045533059
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994432T= , CM000674.2:g.71994432T= GRCh38
NC_000012.11:g.72388212T= , CM000674.1:g.72388212T= GRCh37
NC_000012.10:g.70674479T= NCBI36
NG_008279.1:g.60587T=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.942-7T= MANE Select ENSP00000329093.3:n.942-7T=
ENST00000333850.3:c.942-7T= ENSP00000329093.3:n.942-7T=
NM_173353.3:c.942-7T= NP_775489.2:n.942-7T=
XM_011537899.1:c.348-7T= XP_011536201.1:n.348-7T=
NM_173353.4:c.942-7T= MANE Select NP_775489.2:n.942-7T=
Search 100 bp 5'
Search 100 bp 3'