Canonical Allele Identifier: CA2045533135
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1592402820
gnomAD v4: 12-71994626-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994626C>A , CM000674.2:g.71994626C>A GRCh38
NC_000012.11:g.72388406C>A , CM000674.1:g.72388406C>A GRCh37
NC_000012.10:g.70674673C>A NCBI36
NG_008279.1:g.60781C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1068+61C>A MANE Select ENSP00000329093.3:n.1068+61C>A
ENST00000333850.3:c.1068+61C>A ENSP00000329093.3:n.1068+61C>A
NM_173353.3:c.1068+61C>A NP_775489.2:n.1068+61C>A
XM_011537899.1:c.474+61C>A XP_011536201.1:n.474+61C>A
NM_173353.4:c.1068+61C>A MANE Select NP_775489.2:n.1068+61C>A
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