Canonical Allele Identifier: CA2045509808
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71941926T= , CM000674.2:g.71941926T= GRCh38
NC_000012.11:g.72335706T= , CM000674.1:g.72335706T= GRCh37
NC_000012.10:g.70621973T= NCBI36
NG_008279.1:g.8081T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.255+193T= MANE Select ENSP00000329093.3:n.255+193T=
ENST00000333850.3:c.255+193T= ENSP00000329093.3:n.255+193T=
ENST00000546576.1:n.265+193T=
NM_173353.3:c.255+193T= NP_775489.2:n.255+193T=
XR_245894.2:n.355+193T=
XR_001748575.1:n.355+193T=
NM_173353.4:c.255+193T= MANE Select NP_775489.2:n.255+193T=
Search 100 bp 5'
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