Canonical Allele Identifier: CA480765018
Gene: TPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.72388303G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994523G>T , CM000674.2:g.71994523G>T GRCh38
NC_000012.11:g.72388303G>T , CM000674.1:g.72388303G>T GRCh37
NC_000012.10:g.70674570G>T NCBI36
NG_008279.1:g.60678G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1026G>T MANE Select ENSP00000329093.3:p.Ala342=
ENST00000333850.3:c.1026G>T ENSP00000329093.3:p.Ala342=
NM_173353.3:c.1026G>T NP_775489.2:p.Ala342=
XM_011537899.1:c.432G>T XP_011536201.1:p.Ala144=
NM_173353.4:c.1026G>T MANE Select NP_775489.2:p.Ala342=
Search 100 bp 5'
Search 100 bp 3'