Canonical Allele Identifier: CA2045533048
Gene: TPH2 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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