Canonical Allele Identifier: CA691628226
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1395311553
MyVariant Identifiers: chr12:g.72342310G>A (hg19) chr12:g.71948530G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71948530G>A , CM000674.2:g.71948530G>A GRCh38
NC_000012.11:g.72342310G>A , CM000674.1:g.72342310G>A GRCh37
NC_000012.10:g.70628577G>A NCBI36
NG_008279.1:g.14685G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.541-1058G>A MANE Select ENSP00000329093.3:n.541-1058G>A
ENST00000333850.3:c.541-1058G>A ENSP00000329093.3:n.541-1058G>A
ENST00000546576.1:n.551-1058G>A
NM_173353.3:c.541-1058G>A NP_775489.2:n.541-1058G>A
XM_011537899.1:c.-55+526G>A XP_011536201.1:n.-55+526G>A
XR_245894.2:n.641-1058G>A
XR_001748575.1:n.641-1058G>A
NM_173353.4:c.541-1058G>A MANE Select NP_775489.2:n.541-1058G>A
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