Canonical Allele Identifier: CA385782126
Gene: TPH2 HGNC NCBI

Linked Data

COSMIC: COSM6073632
MyVariant Identifiers: chr12:g.72388308T>G (hg19) chr12:g.71994528T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994528T>G , CM000674.2:g.71994528T>G GRCh38
NC_000012.11:g.72388308T>G , CM000674.1:g.72388308T>G GRCh37
NC_000012.10:g.70674575T>G NCBI36
NG_008279.1:g.60683T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1031T>G MANE Select ENSP00000329093.3:p.Leu344Arg
ENST00000333850.3:c.1031T>G ENSP00000329093.3:p.Leu344Arg
NM_173353.3:c.1031T>G NP_775489.2:p.Leu344Arg
XM_011537899.1:c.437T>G XP_011536201.1:p.Leu146Arg
NM_173353.4:c.1031T>G MANE Select NP_775489.2:p.Leu344Arg
Search 100 bp 5'
Search 100 bp 3'