Canonical Allele Identifier: CA2796494959
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71943053C>A , CM000674.2:g.71943053C>A GRCh38
NC_000012.11:g.72336833C>A , CM000674.1:g.72336833C>A GRCh37
NC_000012.10:g.70623100C>A NCBI36
NG_008279.1:g.9208C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.256-1241C>A MANE Select ENSP00000329093.3:n.256-1241C>A
ENST00000333850.3:c.256-1241C>A ENSP00000329093.3:n.256-1241C>A
ENST00000546576.1:n.266-1241C>A
NM_173353.3:c.256-1241C>A NP_775489.2:n.256-1241C>A
XR_245894.2:n.356-1241C>A
XR_001748575.1:n.356-1241C>A
NM_173353.4:c.256-1241C>A MANE Select NP_775489.2:n.256-1241C>A
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