Canonical Allele Identifier: CA2619886829
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71938875-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938875A>C , CM000674.2:g.71938875A>C GRCh38
NC_000012.11:g.72332655A>C , CM000674.1:g.72332655A>C GRCh37
NC_000012.10:g.70618922A>C NCBI36
NG_008279.1:g.5030A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-112A>C MANE Select ENSP00000329093.3:n.-112A>C
ENST00000333850.3:c.-112A>C ENSP00000329093.3:n.-112A>C
NM_173353.3:c.-112A>C NP_775489.2:n.-112A>C
NM_173353.4:c.-112A>C MANE Select NP_775489.2:n.-112A>C
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