Canonical Allele Identifier: CA385782035
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1872647769
MyVariant Identifiers: chr12:g.72388291A>C (hg19) chr12:g.71994511A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994511A>C , CM000674.2:g.71994511A>C GRCh38
NC_000012.11:g.72388291A>C , CM000674.1:g.72388291A>C GRCh37
NC_000012.10:g.70674558A>C NCBI36
NG_008279.1:g.60666A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1014A>C MANE Select ENSP00000329093.3:p.Glu338Asp
ENST00000333850.3:c.1014A>C ENSP00000329093.3:p.Glu338Asp
NM_173353.3:c.1014A>C NP_775489.2:p.Glu338Asp
XM_011537899.1:c.420A>C XP_011536201.1:p.Glu140Asp
NM_173353.4:c.1014A>C MANE Select NP_775489.2:p.Glu338Asp
Search 100 bp 5'
Search 100 bp 3'