Canonical Allele Identifier: CA691599313
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1345389482
gnomAD v3: 12-72011403-A-T
gnomAD v4: 12-72011403-A-T
MyVariant Identifiers: chr12:g.72405183A>T (hg19) chr12:g.72011403A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72011403A>T , CM000674.2:g.72011403A>T GRCh38
NC_000012.11:g.72405183A>T , CM000674.1:g.72405183A>T GRCh37
NC_000012.10:g.70691450A>T NCBI36
NG_008279.1:g.77558A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-10996A>T MANE Select ENSP00000329093.3:n.1069-10996A>T
ENST00000333850.3:c.1069-10996A>T ENSP00000329093.3:n.1069-10996A>T
NM_173353.3:c.1069-10996A>T NP_775489.2:n.1069-10996A>T
XM_011537899.1:c.475-10996A>T XP_011536201.1:n.475-10996A>T
NM_173353.4:c.1069-10996A>T MANE Select NP_775489.2:n.1069-10996A>T
Search 100 bp 5'
Search 100 bp 3'