Canonical Allele Identifier: CA691624811
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1250115998
MyVariant Identifiers: chr12:g.72336852_72336853insA (hg19) chr12:g.71943072_71943073insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71943074dup , CM000674.2:g.71943074dup GRCh38
NC_000012.11:g.72336854dup , CM000674.1:g.72336854dup GRCh37
NC_000012.10:g.70623121dup NCBI36
NG_008279.1:g.9229dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.256-1220dup MANE Select ENSP00000329093.3:n.256-1220dup
ENST00000333850.3:c.256-1220dup ENSP00000329093.3:n.256-1220dup
ENST00000546576.1:n.266-1220dup
NM_173353.3:c.256-1220dup NP_775489.2:n.256-1220dup
XR_245894.2:n.356-1220dup
XR_001748575.1:n.356-1220dup
NM_173353.4:c.256-1220dup MANE Select NP_775489.2:n.256-1220dup
Search 100 bp 5'
Search 100 bp 3'