Canonical Allele Identifier: CA239222446
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs963468740
gnomAD v4: 12-71938958-T-G
MyVariant Identifiers: chr12:g.72332738T>G (hg19) chr12:g.71938958T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938958T>G , CM000674.2:g.71938958T>G GRCh38
NC_000012.11:g.72332738T>G , CM000674.1:g.72332738T>G GRCh37
NC_000012.10:g.70619005T>G NCBI36
NG_008279.1:g.5113T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-29T>G MANE Select ENSP00000329093.3:n.-29T>G
ENST00000333850.3:c.-29T>G ENSP00000329093.3:n.-29T>G
NM_173353.3:c.-29T>G NP_775489.2:n.-29T>G
XR_245894.2:n.72T>G
XR_001748575.1:n.72T>G
NM_173353.4:c.-29T>G MANE Select NP_775489.2:n.-29T>G
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