Canonical Allele Identifier: CA385782029
Gene: TPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.72388290A>T (hg19) chr12:g.71994510A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994510A>T , CM000674.2:g.71994510A>T GRCh38
NC_000012.11:g.72388290A>T , CM000674.1:g.72388290A>T GRCh37
NC_000012.10:g.70674557A>T NCBI36
NG_008279.1:g.60665A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1013A>T MANE Select ENSP00000329093.3:p.Glu338Val
ENST00000333850.3:c.1013A>T ENSP00000329093.3:p.Glu338Val
NM_173353.3:c.1013A>T NP_775489.2:p.Glu338Val
XM_011537899.1:c.419A>T XP_011536201.1:p.Glu140Val
NM_173353.4:c.1013A>T MANE Select NP_775489.2:p.Glu338Val
Search 100 bp 5'
Search 100 bp 3'