Canonical Allele Identifier: CA691598959
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1336873855
MyVariant Identifiers: chr12:g.72404307C>T (hg19) chr12:g.72010527C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72010527C>T , CM000674.2:g.72010527C>T GRCh38
NC_000012.11:g.72404307C>T , CM000674.1:g.72404307C>T GRCh37
NC_000012.10:g.70690574C>T NCBI36
NG_008279.1:g.76682C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-11872C>T MANE Select ENSP00000329093.3:n.1069-11872C>T
ENST00000333850.3:c.1069-11872C>T ENSP00000329093.3:n.1069-11872C>T
NM_173353.3:c.1069-11872C>T NP_775489.2:n.1069-11872C>T
XM_011537899.1:c.475-11872C>T XP_011536201.1:n.475-11872C>T
NM_173353.4:c.1069-11872C>T MANE Select NP_775489.2:n.1069-11872C>T
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