Canonical Allele Identifier: CA2796494871
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938952C>G , CM000674.2:g.71938952C>G GRCh38
NC_000012.11:g.72332732C>G , CM000674.1:g.72332732C>G GRCh37
NC_000012.10:g.70618999C>G NCBI36
NG_008279.1:g.5107C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-35C>G MANE Select ENSP00000329093.3:n.-35C>G
ENST00000333850.3:c.-35C>G ENSP00000329093.3:n.-35C>G
NM_173353.3:c.-35C>G NP_775489.2:n.-35C>G
XR_245894.2:n.66C>G
XR_001748575.1:n.66C>G
NM_173353.4:c.-35C>G MANE Select NP_775489.2:n.-35C>G