Canonical Allele Identifier: CA691585434
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1248270074
MyVariant Identifiers: chr12:g.72377314G>C (hg19) chr12:g.71983534G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71983534G>C , CM000674.2:g.71983534G>C GRCh38
NC_000012.11:g.72377314G>C , CM000674.1:g.72377314G>C GRCh37
NC_000012.10:g.70663581G>C NCBI36
NG_008279.1:g.49689G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.941+4447G>C MANE Select ENSP00000329093.3:n.941+4447G>C
ENST00000333850.3:c.941+4447G>C ENSP00000329093.3:n.941+4447G>C
NM_173353.3:c.941+4447G>C NP_775489.2:n.941+4447G>C
XM_011537899.1:c.347+4447G>C XP_011536201.1:n.347+4447G>C
NM_173353.4:c.941+4447G>C MANE Select NP_775489.2:n.941+4447G>C
Search 100 bp 5'
Search 100 bp 3'