Canonical Allele Identifier: CA385782079
Gene: TPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.72388299T>A (hg19) chr12:g.71994519T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994519T>A , CM000674.2:g.71994519T>A GRCh38
NC_000012.11:g.72388299T>A , CM000674.1:g.72388299T>A GRCh37
NC_000012.10:g.70674566T>A NCBI36
NG_008279.1:g.60674T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1022T>A MANE Select ENSP00000329093.3:p.Leu341Gln
ENST00000333850.3:c.1022T>A ENSP00000329093.3:p.Leu341Gln
NM_173353.3:c.1022T>A NP_775489.2:p.Leu341Gln
XM_011537899.1:c.428T>A XP_011536201.1:p.Leu143Gln
NM_173353.4:c.1022T>A MANE Select NP_775489.2:p.Leu341Gln
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