Canonical Allele Identifier: CA691623950
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1203031559
gnomAD v3: 12-71941951-G-T
gnomAD v4: 12-71941951-G-T
MyVariant Identifiers: chr12:g.72335731G>T (hg19) chr12:g.71941951G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71941951G>T , CM000674.2:g.71941951G>T GRCh38
NC_000012.11:g.72335731G>T , CM000674.1:g.72335731G>T GRCh37
NC_000012.10:g.70621998G>T NCBI36
NG_008279.1:g.8106G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.255+218G>T MANE Select ENSP00000329093.3:n.255+218G>T
ENST00000333850.3:c.255+218G>T ENSP00000329093.3:n.255+218G>T
ENST00000546576.1:n.265+218G>T
NM_173353.3:c.255+218G>T NP_775489.2:n.255+218G>T
XR_245894.2:n.355+218G>T
XR_001748575.1:n.355+218G>T
NM_173353.4:c.255+218G>T MANE Select NP_775489.2:n.255+218G>T
Search 100 bp 5'
Search 100 bp 3'