Canonical Allele Identifier: CA2575227522
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71938967-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71938967A>G , CM000674.2:g.71938967A>G GRCh38
NC_000012.11:g.72332747A>G , CM000674.1:g.72332747A>G GRCh37
NC_000012.10:g.70619014A>G NCBI36
NG_008279.1:g.5122A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.-20A>G MANE Select ENSP00000329093.3:n.-20A>G
ENST00000333850.3:c.-20A>G ENSP00000329093.3:n.-20A>G
NM_173353.3:c.-20A>G NP_775489.2:n.-20A>G
XR_245894.2:n.81A>G
XR_001748575.1:n.81A>G
NM_173353.4:c.-20A>G MANE Select NP_775489.2:n.-20A>G
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