Canonical Allele Identifier: CA2045515535
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71948425G= , CM000674.2:g.71948425G= GRCh38
NC_000012.11:g.72342205G= , CM000674.1:g.72342205G= GRCh37
NC_000012.10:g.70628472G= NCBI36
NG_008279.1:g.14580G=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.541-1163G= MANE Select ENSP00000329093.3:n.541-1163G=
ENST00000333850.3:c.541-1163G= ENSP00000329093.3:n.541-1163G=
ENST00000546576.1:n.551-1163G=
NM_173353.3:c.541-1163G= NP_775489.2:n.541-1163G=
XM_011537899.1:c.-55+421G= XP_011536201.1:n.-55+421G=
XR_245894.2:n.641-1163G=
XR_001748575.1:n.641-1163G=
NM_173353.4:c.541-1163G= MANE Select NP_775489.2:n.541-1163G=
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