Canonical Allele Identifier: CA239222320
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs112516740
MyVariant Identifiers: chr12:g.72332648T>A (hg19) chr12:g.71938868T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938868T>A , CM000674.2:g.71938868T>A GRCh38
NC_000012.11:g.72332648T>A , CM000674.1:g.72332648T>A GRCh37
NC_000012.10:g.70618915T>A NCBI36
NG_008279.1:g.5023T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-119T>A MANE Select ENSP00000329093.3:n.-119T>A
ENST00000333850.3:c.-119T>A ENSP00000329093.3:n.-119T>A
NM_173353.3:c.-119T>A NP_775489.2:n.-119T>A
NM_173353.4:c.-119T>A MANE Select NP_775489.2:n.-119T>A
Search 100 bp 5'
Search 100 bp 3'