Canonical Allele Identifier: CA691624684
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1202807873
MyVariant Identifiers: chr12:g.72336646G>T (hg19) chr12:g.71942866G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71942866G>T , CM000674.2:g.71942866G>T GRCh38
NC_000012.11:g.72336646G>T , CM000674.1:g.72336646G>T GRCh37
NC_000012.10:g.70622913G>T NCBI36
NG_008279.1:g.9021G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.255+1133G>T MANE Select ENSP00000329093.3:n.255+1133G>T
ENST00000333850.3:c.255+1133G>T ENSP00000329093.3:n.255+1133G>T
ENST00000546576.1:n.265+1133G>T
NM_173353.3:c.255+1133G>T NP_775489.2:n.255+1133G>T
XR_245894.2:n.355+1133G>T
XR_001748575.1:n.355+1133G>T
NM_173353.4:c.255+1133G>T MANE Select NP_775489.2:n.255+1133G>T
Search 100 bp 5'
Search 100 bp 3'