Canonical Allele Identifier: CA385782027
Gene: TPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.72388290A>C (hg19) chr12:g.71994510A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994510A>C , CM000674.2:g.71994510A>C GRCh38
NC_000012.11:g.72388290A>C , CM000674.1:g.72388290A>C GRCh37
NC_000012.10:g.70674557A>C NCBI36
NG_008279.1:g.60665A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1013A>C MANE Select ENSP00000329093.3:p.Glu338Ala
ENST00000333850.3:c.1013A>C ENSP00000329093.3:p.Glu338Ala
NM_173353.3:c.1013A>C NP_775489.2:p.Glu338Ala
XM_011537899.1:c.419A>C XP_011536201.1:p.Glu140Ala
NM_173353.4:c.1013A>C MANE Select NP_775489.2:p.Glu338Ala
Search 100 bp 5'
Search 100 bp 3'