Canonical Allele Identifier: CA385781733
Gene: TPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.72388218G>T (hg19) chr12:g.71994438G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994438G>T , CM000674.2:g.71994438G>T GRCh38
NC_000012.11:g.72388218G>T , CM000674.1:g.72388218G>T GRCh37
NC_000012.10:g.70674485G>T NCBI36
NG_008279.1:g.60593G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.942-1G>T MANE Select ENSP00000329093.3:n.942-1G>T
ENST00000333850.3:c.942-1G>T ENSP00000329093.3:n.942-1G>T
NM_173353.3:c.942-1G>T NP_775489.2:n.942-1G>T
XM_011537899.1:c.348-1G>T XP_011536201.1:n.348-1G>T
NM_173353.4:c.942-1G>T MANE Select NP_775489.2:n.942-1G>T
Search 100 bp 5'
Search 100 bp 3'