Canonical Allele Identifier: CA2045509846
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71941974C= , CM000674.2:g.71941974C= GRCh38
NC_000012.11:g.72335754C= , CM000674.1:g.72335754C= GRCh37
NC_000012.10:g.70622021C= NCBI36
NG_008279.1:g.8129C=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.255+241C= MANE Select ENSP00000329093.3:n.255+241C=
ENST00000333850.3:c.255+241C= ENSP00000329093.3:n.255+241C=
ENST00000546576.1:n.265+241C=
NM_173353.3:c.255+241C= NP_775489.2:n.255+241C=
XR_245894.2:n.355+241C=
XR_001748575.1:n.355+241C=
NM_173353.4:c.255+241C= MANE Select NP_775489.2:n.255+241C=
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