Canonical Allele Identifier: CA2619886905
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71938960-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938960C>A , CM000674.2:g.71938960C>A GRCh38
NC_000012.11:g.72332740C>A , CM000674.1:g.72332740C>A GRCh37
NC_000012.10:g.70619007C>A NCBI36
NG_008279.1:g.5115C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-27C>A MANE Select ENSP00000329093.3:n.-27C>A
ENST00000333850.3:c.-27C>A ENSP00000329093.3:n.-27C>A
NM_173353.3:c.-27C>A NP_775489.2:n.-27C>A
XR_245894.2:n.74C>A
XR_001748575.1:n.74C>A
NM_173353.4:c.-27C>A MANE Select NP_775489.2:n.-27C>A
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