Canonical Allele Identifier: CA691621156
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1424921675
gnomAD v3: 12-71938867-T-G
gnomAD v4: 12-71938867-T-G
MyVariant Identifiers: chr12:g.72332647T>G (hg19) chr12:g.71938867T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938867T>G , CM000674.2:g.71938867T>G GRCh38
NC_000012.11:g.72332647T>G , CM000674.1:g.72332647T>G GRCh37
NC_000012.10:g.70618914T>G NCBI36
NG_008279.1:g.5022T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-120T>G MANE Select ENSP00000329093.3:n.-120T>G
ENST00000333850.3:c.-120T>G ENSP00000329093.3:n.-120T>G
NM_173353.3:c.-120T>G NP_775489.2:n.-120T>G
NM_173353.4:c.-120T>G MANE Select NP_775489.2:n.-120T>G
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