Canonical Allele Identifier: CA2045515613
Gene: TPH2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71948506A= , CM000674.2:g.71948506A= GRCh38
NC_000012.11:g.72342286A= , CM000674.1:g.72342286A= GRCh37
NC_000012.10:g.70628553A= NCBI36
NG_008279.1:g.14661A=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.541-1082A= MANE Select ENSP00000329093.3:n.541-1082A=
ENST00000333850.3:c.541-1082A= ENSP00000329093.3:n.541-1082A=
ENST00000546576.1:n.551-1082A=
NM_173353.3:c.541-1082A= NP_775489.2:n.541-1082A=
XM_011537899.1:c.-55+502A= XP_011536201.1:n.-55+502A=
XR_245894.2:n.641-1082A=
XR_001748575.1:n.641-1082A=
NM_173353.4:c.541-1082A= MANE Select NP_775489.2:n.541-1082A=
Search 100 bp 5'
Search 100 bp 3'