Canonical Allele Identifier: CA385782150
Gene: TPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.72388313G>C (hg19) chr12:g.71994533G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994533G>C , CM000674.2:g.71994533G>C GRCh38
NC_000012.11:g.72388313G>C , CM000674.1:g.72388313G>C GRCh37
NC_000012.10:g.70674580G>C NCBI36
NG_008279.1:g.60688G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1036G>C MANE Select ENSP00000329093.3:p.Ala346Pro
ENST00000333850.3:c.1036G>C ENSP00000329093.3:p.Ala346Pro
NM_173353.3:c.1036G>C NP_775489.2:p.Ala346Pro
XM_011537899.1:c.442G>C XP_011536201.1:p.Ala148Pro
NM_173353.4:c.1036G>C MANE Select NP_775489.2:p.Ala346Pro
Search 100 bp 5'
Search 100 bp 3'