Canonical Allele Identifier: CA691621133

Gene: TPH2

Linked Data

• dbSNP Id: rs961225966
• gnomAD v3: 12-71938845-G-T
• gnomAD v4: 12-71938845-G-T
• MyVariant Identifiers: chr12:g.72332625G>T (hg19) ; chr12:g.71938845G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71938845G>T , CM000674.2:g.71938845G>T	GRCh38
NC_000012.11:g.72332625G>T , CM000674.1:g.72332625G>T	GRCh37
NC_000012.10:g.70618892G>T	NCBI36
NG_008279.1:g.5000G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333850.4:c.-142G>T MANE Select	ENSP00000329093.3:n.-142G>T
NM_173353.4:c.-142G>T MANE Select	NP_775489.2:n.-142G>T