Canonical Allele Identifier: CA2580601894

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72020783A>C , CM000674.2:g.72020783A>C	GRCh38
NC_000012.11:g.72414563A>C , CM000674.1:g.72414563A>C	GRCh37
NC_000012.10:g.70700830A>C	NCBI36
NG_008279.1:g.86938A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.1069-1616A>C MANE Select	ENSP00000329093.3:n.1069-1616A>C
ENST00000333850.3:c.1069-1616A>C	ENSP00000329093.3:n.1069-1616A>C
NM_173353.3:c.1069-1616A>C	NP_775489.2:n.1069-1616A>C
XM_011537899.1:c.475-1616A>C	XP_011536201.1:n.475-1616A>C
NM_173353.4:c.1069-1616A>C MANE Select	NP_775489.2:n.1069-1616A>C