Canonical Allele Identifier: CA2796494863
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938870T>G , CM000674.2:g.71938870T>G GRCh38
NC_000012.11:g.72332650T>G , CM000674.1:g.72332650T>G GRCh37
NC_000012.10:g.70618917T>G NCBI36
NG_008279.1:g.5025T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-117T>G MANE Select ENSP00000329093.3:n.-117T>G
ENST00000333850.3:c.-117T>G ENSP00000329093.3:n.-117T>G
NM_173353.3:c.-117T>G NP_775489.2:n.-117T>G
NM_173353.4:c.-117T>G MANE Select NP_775489.2:n.-117T>G