Canonical Allele Identifier: CA2045509839
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71941970A= , CM000674.2:g.71941970A= GRCh38
NC_000012.11:g.72335750A= , CM000674.1:g.72335750A= GRCh37
NC_000012.10:g.70622017A= NCBI36
NG_008279.1:g.8125A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.255+237A= MANE Select ENSP00000329093.3:n.255+237A=
ENST00000333850.3:c.255+237A= ENSP00000329093.3:n.255+237A=
ENST00000546576.1:n.265+237A=
NM_173353.3:c.255+237A= NP_775489.2:n.255+237A=
XR_245894.2:n.355+237A=
XR_001748575.1:n.355+237A=
NM_173353.4:c.255+237A= MANE Select NP_775489.2:n.255+237A=
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