Canonical Allele Identifier: CA2598986645
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs2139182891
gnomAD v3: 12-71948422-A-G
gnomAD v4: 12-71948422-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71948422A>G , CM000674.2:g.71948422A>G GRCh38
NC_000012.11:g.72342202A>G , CM000674.1:g.72342202A>G GRCh37
NC_000012.10:g.70628469A>G NCBI36
NG_008279.1:g.14577A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.541-1166A>G MANE Select ENSP00000329093.3:n.541-1166A>G
ENST00000333850.3:c.541-1166A>G ENSP00000329093.3:n.541-1166A>G
ENST00000546576.1:n.551-1166A>G
NM_173353.3:c.541-1166A>G NP_775489.2:n.541-1166A>G
XM_011537899.1:c.-55+418A>G XP_011536201.1:n.-55+418A>G
XR_245894.2:n.641-1166A>G
XR_001748575.1:n.641-1166A>G
NM_173353.4:c.541-1166A>G MANE Select NP_775489.2:n.541-1166A>G
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