Canonical Allele Identifier: CA2045506537
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938867T= , CM000674.2:g.71938867T= GRCh38
NC_000012.11:g.72332647T= , CM000674.1:g.72332647T= GRCh37
NC_000012.10:g.70618914T= NCBI36
NG_008279.1:g.5022T=

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-120T= MANE Select ENSP00000329093.3:n.-120T=
ENST00000333850.3:c.-120T= ENSP00000329093.3:n.-120T=
NM_173353.3:c.-120T= NP_775489.2:n.-120T=
NM_173353.4:c.-120T= MANE Select NP_775489.2:n.-120T=
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