Canonical Allele Identifier: CA239237766
Gene: TPH2 HGNC NCBI
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72018792T>G , CM000674.2:g.72018792T>G GRCh38
NC_000012.11:g.72412572T>G , CM000674.1:g.72412572T>G GRCh37
NC_000012.10:g.70698839T>G NCBI36
NG_008279.1:g.84947T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-3607T>G MANE Select ENSP00000329093.3:n.1069-3607T>G
ENST00000333850.3:c.1069-3607T>G ENSP00000329093.3:n.1069-3607T>G
NM_173353.3:c.1069-3607T>G NP_775489.2:n.1069-3607T>G
XM_011537899.1:c.475-3607T>G XP_011536201.1:n.475-3607T>G
NM_173353.4:c.1069-3607T>G MANE Select NP_775489.2:n.1069-3607T>G