Canonical Allele Identifier: CA2045515567
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71948467G= , CM000674.2:g.71948467G= GRCh38
NC_000012.11:g.72342247G= , CM000674.1:g.72342247G= GRCh37
NC_000012.10:g.70628514G= NCBI36
NG_008279.1:g.14622G=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.541-1121G= MANE Select ENSP00000329093.3:n.541-1121G=
ENST00000333850.3:c.541-1121G= ENSP00000329093.3:n.541-1121G=
ENST00000546576.1:n.551-1121G=
NM_173353.3:c.541-1121G= NP_775489.2:n.541-1121G=
XM_011537899.1:c.-55+463G= XP_011536201.1:n.-55+463G=
XR_245894.2:n.641-1121G=
XR_001748575.1:n.641-1121G=
NM_173353.4:c.541-1121G= MANE Select NP_775489.2:n.541-1121G=
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