Canonical Allele Identifier: CA480768918
Gene: TPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.72416241A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72022461A>G , CM000674.2:g.72022461A>G GRCh38
NC_000012.11:g.72416241A>G , CM000674.1:g.72416241A>G GRCh37
NC_000012.10:g.70702508A>G NCBI36
NG_008279.1:g.88616A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1131A>G MANE Select ENSP00000329093.3:p.Gly377=
ENST00000333850.3:c.1131A>G ENSP00000329093.3:p.Gly377=
NM_173353.3:c.1131A>G NP_775489.2:p.Gly377=
XM_011537899.1:c.537A>G XP_011536201.1:p.Gly179=
NM_173353.4:c.1131A>G MANE Select NP_775489.2:p.Gly377=
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