Canonical Allele Identifier: CA2045506683
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938950C= , CM000674.2:g.71938950C= GRCh38
NC_000012.11:g.72332730C= , CM000674.1:g.72332730C= GRCh37
NC_000012.10:g.70618997C= NCBI36
NG_008279.1:g.5105C=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-37C= MANE Select ENSP00000329093.3:n.-37C=
ENST00000333850.3:c.-37C= ENSP00000329093.3:n.-37C=
NM_173353.3:c.-37C= NP_775489.2:n.-37C=
XR_245894.2:n.64C=
XR_001748575.1:n.64C=
NM_173353.4:c.-37C= MANE Select NP_775489.2:n.-37C=