Canonical Allele Identifier: CA2619886892
Gene: TPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938937T>C , CM000674.2:g.71938937T>C GRCh38
NC_000012.11:g.72332717T>C , CM000674.1:g.72332717T>C GRCh37
NC_000012.10:g.70618984T>C NCBI36
NG_008279.1:g.5092T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-50T>C MANE Select ENSP00000329093.3:n.-50T>C
ENST00000333850.3:c.-50T>C ENSP00000329093.3:n.-50T>C
NM_173353.3:c.-50T>C NP_775489.2:n.-50T>C
XR_245894.2:n.51T>C
XR_001748575.1:n.51T>C
NM_173353.4:c.-50T>C MANE Select NP_775489.2:n.-50T>C