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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:
CA365338660
Gene: FOXO3
HGNC
NCBI
Linked Data
gnomAD v4:
6-108561710-C-T
MyVariant Identifiers:
chr6:g.108882913C>T (hg19)
chr6:g.108561710C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.108561710C>T , CM000668.2:g.108561710C>T
GRCh38
NC_000006.11:g.108882913C>T , CM000668.1:g.108882913C>T
GRCh37
NC_000006.10:g.108989606C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000406360.2:c.502C>T
MANE Select
ENSP00000385824.1:p.Arg168Cys
ENST00000343882.10:c.502C>T
ENSP00000339527.6:p.Arg168Cys
ENST00000406360.1:c.502C>T
ENSP00000385824.1:p.Arg168Cys
NM_001455.3:c.502C>T
NP_001446.1:p.Arg168Cys
NM_201559.2:c.502C>T
NP_963853.1:p.Arg168Cys
NM_001455.4:c.502C>T
MANE Select
NP_001446.1:p.Arg168Cys
NM_201559.3:c.502C>T
NP_963853.1:p.Arg168Cys
Search 100 bp 5'
Search 100 bp 3'