Canonical Allele Identifier: CA480764965
Gene: TPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.72388219A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994439A>C , CM000674.2:g.71994439A>C GRCh38
NC_000012.11:g.72388219A>C , CM000674.1:g.72388219A>C GRCh37
NC_000012.10:g.70674486A>C NCBI36
NG_008279.1:g.60594A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.942A>C MANE Select ENSP00000329093.3:p.Pro314=
ENST00000333850.3:c.942A>C ENSP00000329093.3:p.Pro314=
NM_173353.3:c.942A>C NP_775489.2:p.Pro314=
XM_011537899.1:c.348A>C XP_011536201.1:p.Pro116=
NM_173353.4:c.942A>C MANE Select NP_775489.2:p.Pro314=
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