Canonical Allele Identifier: CA239239579
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs190406451
gnomAD v2: 12-72414559-G-A
gnomAD v3: 12-72020779-G-A
gnomAD v4: 12-72020779-G-A
MyVariant Identifiers: chr12:g.72414559G>A (hg19) chr12:g.72020779G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020779G>A , CM000674.2:g.72020779G>A GRCh38
NC_000012.11:g.72414559G>A , CM000674.1:g.72414559G>A GRCh37
NC_000012.10:g.70700826G>A NCBI36
NG_008279.1:g.86934G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1620G>A MANE Select ENSP00000329093.3:n.1069-1620G>A
ENST00000333850.3:c.1069-1620G>A ENSP00000329093.3:n.1069-1620G>A
NM_173353.3:c.1069-1620G>A NP_775489.2:n.1069-1620G>A
XM_011537899.1:c.475-1620G>A XP_011536201.1:n.475-1620G>A
NM_173353.4:c.1069-1620G>A MANE Select NP_775489.2:n.1069-1620G>A
Search 100 bp 5'
Search 100 bp 3'