Canonical Allele Identifier: CA605810910
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1397997455
gnomAD v2: 12-72388395-G-C
gnomAD v4: 12-71994615-G-C
MyVariant Identifiers: chr12:g.72388395G>C (hg19) chr12:g.71994615G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994615G>C , CM000674.2:g.71994615G>C GRCh38
NC_000012.11:g.72388395G>C , CM000674.1:g.72388395G>C GRCh37
NC_000012.10:g.70674662G>C NCBI36
NG_008279.1:g.60770G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1068+50G>C MANE Select ENSP00000329093.3:n.1068+50G>C
ENST00000333850.3:c.1068+50G>C ENSP00000329093.3:n.1068+50G>C
NM_173353.3:c.1068+50G>C NP_775489.2:n.1068+50G>C
XM_011537899.1:c.474+50G>C XP_011536201.1:n.474+50G>C
NM_173353.4:c.1068+50G>C MANE Select NP_775489.2:n.1068+50G>C
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