Canonical Allele Identifier: CA239224441
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1022258432
MyVariant Identifiers: chr12:g.72336758T>C (hg19) chr12:g.71942978T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71942978T>C , CM000674.2:g.71942978T>C GRCh38
NC_000012.11:g.72336758T>C , CM000674.1:g.72336758T>C GRCh37
NC_000012.10:g.70623025T>C NCBI36
NG_008279.1:g.9133T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.255+1245T>C MANE Select ENSP00000329093.3:n.255+1245T>C
ENST00000333850.3:c.255+1245T>C ENSP00000329093.3:n.255+1245T>C
ENST00000546576.1:n.265+1245T>C
NM_173353.3:c.255+1245T>C NP_775489.2:n.255+1245T>C
XR_245894.2:n.355+1245T>C
XR_001748575.1:n.355+1245T>C
NM_173353.4:c.255+1245T>C MANE Select NP_775489.2:n.255+1245T>C
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