Canonical Allele Identifier: CA2045533127
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994607A= , CM000674.2:g.71994607A= GRCh38
NC_000012.11:g.72388387A= , CM000674.1:g.72388387A= GRCh37
NC_000012.10:g.70674654A= NCBI36
NG_008279.1:g.60762A=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1068+42A= MANE Select ENSP00000329093.3:n.1068+42A=
ENST00000333850.3:c.1068+42A= ENSP00000329093.3:n.1068+42A=
NM_173353.3:c.1068+42A= NP_775489.2:n.1068+42A=
XM_011537899.1:c.474+42A= XP_011536201.1:n.474+42A=
NM_173353.4:c.1068+42A= MANE Select NP_775489.2:n.1068+42A=