Canonical Allele Identifier: CA949093615
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1173580690
gnomAD v3: 12-72010547-G-C
gnomAD v4: 12-72010547-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72010547G>C , CM000674.2:g.72010547G>C GRCh38
NC_000012.11:g.72404327G>C , CM000674.1:g.72404327G>C GRCh37
NC_000012.10:g.70690594G>C NCBI36
NG_008279.1:g.76702G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-11852G>C MANE Select ENSP00000329093.3:n.1069-11852G>C
ENST00000333850.3:c.1069-11852G>C ENSP00000329093.3:n.1069-11852G>C
NM_173353.3:c.1069-11852G>C NP_775489.2:n.1069-11852G>C
XM_011537899.1:c.475-11852G>C XP_011536201.1:n.475-11852G>C
NM_173353.4:c.1069-11852G>C MANE Select NP_775489.2:n.1069-11852G>C
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