Canonical Allele Identifier: CA239219062

Gene: TPH2

Linked Data

• dbSNP Id: rs1015666671
• MyVariant Identifiers: chr12:g.72377216C>T (hg19) ; chr12:g.71983436C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71983436C>T , CM000674.2:g.71983436C>T	GRCh38
NC_000012.11:g.72377216C>T , CM000674.1:g.72377216C>T	GRCh37
NC_000012.10:g.70663483C>T	NCBI36
NG_008279.1:g.49591C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333850.4:c.941+4349C>T MANE Select	ENSP00000329093.3:n.941+4349C>T
ENST00000333850.3:c.941+4349C>T	ENSP00000329093.3:n.941+4349C>T
NM_173353.3:c.941+4349C>T	NP_775489.2:n.941+4349C>T
XM_011537899.1:c.347+4349C>T	XP_011536201.1:n.347+4349C>T
NM_173353.4:c.941+4349C>T MANE Select	NP_775489.2:n.941+4349C>T