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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA480765017
Gene: TPH2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr12:g.72388303G>C (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.71994523G>C , CM000674.2:g.71994523G>C
GRCh38
NC_000012.11:g.72388303G>C , CM000674.1:g.72388303G>C
GRCh37
NC_000012.10:g.70674570G>C
NCBI36
NG_008279.1:g.60678G>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000333850.4:c.1026G>C
MANE Select
ENSP00000329093.3:p.Ala342=
ENST00000333850.3:c.1026G>C
ENSP00000329093.3:p.Ala342=
NM_173353.3:c.1026G>C
NP_775489.2:p.Ala342=
XM_011537899.1:c.432G>C
XP_011536201.1:p.Ala144=
NM_173353.4:c.1026G>C
MANE Select
NP_775489.2:p.Ala342=
Search 100 bp 5'
Search 100 bp 3'