Canonical Allele Identifier: CA691623939

Gene: TPH2

Linked Data

• dbSNP Id: rs1480589767
• gnomAD v3: 12-71941926-T-C
• gnomAD v4: 12-71941926-T-C
• MyVariant Identifiers: chr12:g.72335706T>C (hg19) ; chr12:g.71941926T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71941926T>C , CM000674.2:g.71941926T>C	GRCh38
NC_000012.11:g.72335706T>C , CM000674.1:g.72335706T>C	GRCh37
NC_000012.10:g.70621973T>C	NCBI36
NG_008279.1:g.8081T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.255+193T>C MANE Select	ENSP00000329093.3:n.255+193T>C
ENST00000333850.3:c.255+193T>C	ENSP00000329093.3:n.255+193T>C
ENST00000546576.1:n.265+193T>C
NM_173353.3:c.255+193T>C	NP_775489.2:n.255+193T>C
XR_245894.2:n.355+193T>C
XR_001748575.1:n.355+193T>C
NM_173353.4:c.255+193T>C MANE Select	NP_775489.2:n.255+193T>C