Canonical Allele Identifier: CA239232934
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs867172628
gnomAD v2: 12-72404895-G-T
gnomAD v3: 12-72011115-G-T
gnomAD v4: 12-72011115-G-T
MyVariant Identifiers: chr12:g.72404895G>T (hg19) chr12:g.72404895_72404902delinsTGTAGCTA (hg19) chr12:g.72011115G>T (hg38) chr12:g.72011115_72011122delinsTGTAGCTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72011115G>T , CM000674.2:g.72011115G>T GRCh38
NC_000012.11:g.72404895G>T , CM000674.1:g.72404895G>T GRCh37
NC_000012.10:g.70691162G>T NCBI36
NG_008279.1:g.77270G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-11284G>T MANE Select ENSP00000329093.3:n.1069-11284G>T
ENST00000333850.3:c.1069-11284G>T ENSP00000329093.3:n.1069-11284G>T
NM_173353.3:c.1069-11284G>T NP_775489.2:n.1069-11284G>T
XM_011537899.1:c.475-11284G>T XP_011536201.1:n.475-11284G>T
NM_173353.4:c.1069-11284G>T MANE Select NP_775489.2:n.1069-11284G>T
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