Canonical Allele Identifier: CA2619886906

Gene: TPH2

Linked Data

• gnomAD v4: 12-71938961-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71938961A>C , CM000674.2:g.71938961A>C	GRCh38
NC_000012.11:g.72332741A>C , CM000674.1:g.72332741A>C	GRCh37
NC_000012.10:g.70619008A>C	NCBI36
NG_008279.1:g.5116A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.-26A>C MANE Select	ENSP00000329093.3:n.-26A>C
ENST00000333850.3:c.-26A>C	ENSP00000329093.3:n.-26A>C
NM_173353.3:c.-26A>C	NP_775489.2:n.-26A>C
XR_245894.2:n.75A>C
XR_001748575.1:n.75A>C
NM_173353.4:c.-26A>C MANE Select	NP_775489.2:n.-26A>C