Canonical Allele Identifier: CA949084617
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1872344025
gnomAD v3: 12-71983466-A-C
gnomAD v4: 12-71983466-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71983466A>C , CM000674.2:g.71983466A>C GRCh38
NC_000012.11:g.72377246A>C , CM000674.1:g.72377246A>C GRCh37
NC_000012.10:g.70663513A>C NCBI36
NG_008279.1:g.49621A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.941+4379A>C MANE Select ENSP00000329093.3:n.941+4379A>C
ENST00000333850.3:c.941+4379A>C ENSP00000329093.3:n.941+4379A>C
NM_173353.3:c.941+4379A>C NP_775489.2:n.941+4379A>C
XM_011537899.1:c.347+4379A>C XP_011536201.1:n.347+4379A>C
NM_173353.4:c.941+4379A>C MANE Select NP_775489.2:n.941+4379A>C
Search 100 bp 5'
Search 100 bp 3'