Canonical Allele Identifier: CA385782016
Gene: TPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994508A>T , CM000674.2:g.71994508A>T GRCh38
NC_000012.11:g.72388288A>T , CM000674.1:g.72388288A>T GRCh37
NC_000012.10:g.70674555A>T NCBI36
NG_008279.1:g.60663A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1011A>T MANE Select ENSP00000329093.3:p.Gln337His
ENST00000333850.3:c.1011A>T ENSP00000329093.3:p.Gln337His
NM_173353.3:c.1011A>T NP_775489.2:p.Gln337His
XM_011537899.1:c.417A>T XP_011536201.1:p.Gln139His
NM_173353.4:c.1011A>T MANE Select NP_775489.2:p.Gln337His