Canonical Allele Identifier: CA2045533133
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994626C= , CM000674.2:g.71994626C= GRCh38
NC_000012.11:g.72388406C= , CM000674.1:g.72388406C= GRCh37
NC_000012.10:g.70674673C= NCBI36
NG_008279.1:g.60781C=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1068+61C= MANE Select ENSP00000329093.3:n.1068+61C=
ENST00000333850.3:c.1068+61C= ENSP00000329093.3:n.1068+61C=
NM_173353.3:c.1068+61C= NP_775489.2:n.1068+61C=
XM_011537899.1:c.474+61C= XP_011536201.1:n.474+61C=
NM_173353.4:c.1068+61C= MANE Select NP_775489.2:n.1068+61C=