Canonical Allele Identifier: CA239223972
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs924024707
gnomAD v2: 12-72335722-A-G
gnomAD v3: 12-71941942-A-G
gnomAD v4: 12-71941942-A-G
MyVariant Identifiers: chr12:g.72335722A>G (hg19) chr12:g.71941942A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71941942A>G , CM000674.2:g.71941942A>G GRCh38
NC_000012.11:g.72335722A>G , CM000674.1:g.72335722A>G GRCh37
NC_000012.10:g.70621989A>G NCBI36
NG_008279.1:g.8097A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.255+209A>G MANE Select ENSP00000329093.3:n.255+209A>G
ENST00000333850.3:c.255+209A>G ENSP00000329093.3:n.255+209A>G
ENST00000546576.1:n.265+209A>G
NM_173353.3:c.255+209A>G NP_775489.2:n.255+209A>G
XR_245894.2:n.355+209A>G
XR_001748575.1:n.355+209A>G
NM_173353.4:c.255+209A>G MANE Select NP_775489.2:n.255+209A>G
Search 100 bp 5'
Search 100 bp 3'