Canonical Allele Identifier: CA385782046
Gene: TPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994512A>T , CM000674.2:g.71994512A>T GRCh38
NC_000012.11:g.72388292A>T , CM000674.1:g.72388292A>T GRCh37
NC_000012.10:g.70674559A>T NCBI36
NG_008279.1:g.60667A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1015A>T MANE Select ENSP00000329093.3:p.Ile339Leu
ENST00000333850.3:c.1015A>T ENSP00000329093.3:p.Ile339Leu
NM_173353.3:c.1015A>T NP_775489.2:p.Ile339Leu
XM_011537899.1:c.421A>T XP_011536201.1:p.Ile141Leu
NM_173353.4:c.1015A>T MANE Select NP_775489.2:p.Ile339Leu