Canonical Allele Identifier: CA2796494870
Gene: TPH2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938947G>T , CM000674.2:g.71938947G>T GRCh38
NC_000012.11:g.72332727G>T , CM000674.1:g.72332727G>T GRCh37
NC_000012.10:g.70618994G>T NCBI36
NG_008279.1:g.5102G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-40G>T MANE Select ENSP00000329093.3:n.-40G>T
ENST00000333850.3:c.-40G>T ENSP00000329093.3:n.-40G>T
NM_173353.3:c.-40G>T NP_775489.2:n.-40G>T
XR_245894.2:n.61G>T
XR_001748575.1:n.61G>T
NM_173353.4:c.-40G>T MANE Select NP_775489.2:n.-40G>T
Search 100 bp 5'
Search 100 bp 3'