Canonical Allele Identifier: CA2575227520
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938949A>T , CM000674.2:g.71938949A>T GRCh38
NC_000012.11:g.72332729A>T , CM000674.1:g.72332729A>T GRCh37
NC_000012.10:g.70618996A>T NCBI36
NG_008279.1:g.5104A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-38A>T MANE Select ENSP00000329093.3:n.-38A>T
ENST00000333850.3:c.-38A>T ENSP00000329093.3:n.-38A>T
NM_173353.3:c.-38A>T NP_775489.2:n.-38A>T
XR_245894.2:n.63A>T
XR_001748575.1:n.63A>T
NM_173353.4:c.-38A>T MANE Select NP_775489.2:n.-38A>T