Canonical Allele Identifier: CA239224476
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs952182891
gnomAD v2: 12-72336834-C-T
gnomAD v3: 12-71943054-C-T
gnomAD v4: 12-71943054-C-T
MyVariant Identifiers: chr12:g.72336834C>T (hg19) chr12:g.71943054C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71943054C>T , CM000674.2:g.71943054C>T GRCh38
NC_000012.11:g.72336834C>T , CM000674.1:g.72336834C>T GRCh37
NC_000012.10:g.70623101C>T NCBI36
NG_008279.1:g.9209C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.256-1240C>T MANE Select ENSP00000329093.3:n.256-1240C>T
ENST00000333850.3:c.256-1240C>T ENSP00000329093.3:n.256-1240C>T
ENST00000546576.1:n.266-1240C>T
NM_173353.3:c.256-1240C>T NP_775489.2:n.256-1240C>T
XR_245894.2:n.356-1240C>T
XR_001748575.1:n.356-1240C>T
NM_173353.4:c.256-1240C>T MANE Select NP_775489.2:n.256-1240C>T
Search 100 bp 5'
Search 100 bp 3'