Canonical Allele Identifier: CA691624801
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs145096178
MyVariant Identifiers: chr12:g.72336839G>A (hg19) chr12:g.71943059G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71943059G>A , CM000674.2:g.71943059G>A GRCh38
NC_000012.11:g.72336839G>A , CM000674.1:g.72336839G>A GRCh37
NC_000012.10:g.70623106G>A NCBI36
NG_008279.1:g.9214G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.256-1235G>A MANE Select ENSP00000329093.3:n.256-1235G>A
ENST00000333850.3:c.256-1235G>A ENSP00000329093.3:n.256-1235G>A
ENST00000546576.1:n.266-1235G>A
NM_173353.3:c.256-1235G>A NP_775489.2:n.256-1235G>A
XR_245894.2:n.356-1235G>A
XR_001748575.1:n.356-1235G>A
NM_173353.4:c.256-1235G>A MANE Select NP_775489.2:n.256-1235G>A
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