Canonical Allele Identifier: CA2619886904
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71938957-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938957C>T , CM000674.2:g.71938957C>T GRCh38
NC_000012.11:g.72332737C>T , CM000674.1:g.72332737C>T GRCh37
NC_000012.10:g.70619004C>T NCBI36
NG_008279.1:g.5112C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-30C>T MANE Select ENSP00000329093.3:n.-30C>T
ENST00000333850.3:c.-30C>T ENSP00000329093.3:n.-30C>T
NM_173353.3:c.-30C>T NP_775489.2:n.-30C>T
XR_245894.2:n.71C>T
XR_001748575.1:n.71C>T
NM_173353.4:c.-30C>T MANE Select NP_775489.2:n.-30C>T
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