Canonical Allele Identifier: CA2619868076
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71994621-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994621G>A , CM000674.2:g.71994621G>A GRCh38
NC_000012.11:g.72388401G>A , CM000674.1:g.72388401G>A GRCh37
NC_000012.10:g.70674668G>A NCBI36
NG_008279.1:g.60776G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1068+56G>A MANE Select ENSP00000329093.3:n.1068+56G>A
ENST00000333850.3:c.1068+56G>A ENSP00000329093.3:n.1068+56G>A
NM_173353.3:c.1068+56G>A NP_775489.2:n.1068+56G>A
XM_011537899.1:c.474+56G>A XP_011536201.1:n.474+56G>A
NM_173353.4:c.1068+56G>A MANE Select NP_775489.2:n.1068+56G>A
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