Canonical Allele Identifier: CA385781735
Gene: TPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994440G>A , CM000674.2:g.71994440G>A GRCh38
NC_000012.11:g.72388220G>A , CM000674.1:g.72388220G>A GRCh37
NC_000012.10:g.70674487G>A NCBI36
NG_008279.1:g.60595G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.943G>A MANE Select ENSP00000329093.3:p.Asp315Asn
ENST00000333850.3:c.943G>A ENSP00000329093.3:p.Asp315Asn
NM_173353.3:c.943G>A NP_775489.2:p.Asp315Asn
XM_011537899.1:c.349G>A XP_011536201.1:p.Asp117Asn
NM_173353.4:c.943G>A MANE Select NP_775489.2:p.Asp315Asn