Canonical Allele Identifier: CA2045506547
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1870971517
gnomAD v4: 12-71938874-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938874C>T , CM000674.2:g.71938874C>T GRCh38
NC_000012.11:g.72332654C>T , CM000674.1:g.72332654C>T GRCh37
NC_000012.10:g.70618921C>T NCBI36
NG_008279.1:g.5029C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.-113C>T MANE Select ENSP00000329093.3:n.-113C>T
ENST00000333850.3:c.-113C>T ENSP00000329093.3:n.-113C>T
NM_173353.3:c.-113C>T NP_775489.2:n.-113C>T
NM_173353.4:c.-113C>T MANE Select NP_775489.2:n.-113C>T
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