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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:
CA354705559
Gene: FOXL2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2245675
ClinVar RCV Id:
RCV002733114
MyVariant Identifiers:
chr3:g.138665014T>G (hg19)
chr3:g.138946172T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.138946172T>G , CM000665.2:g.138946172T>G
GRCh38
NC_000003.11:g.138665014T>G , CM000665.1:g.138665014T>G
GRCh37
NC_000003.10:g.140147704T>G
NCBI36
NG_012454.1:g.5969A>C
NG_029796.1:g.3939T>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000648323.1:c.551A>C
MANE Select
ENSP00000497217.1:p.Asp184Ala
ENST00000330315.3:c.551A>C
ENSP00000333188.3:p.Asp184Ala
NM_023067.3:c.551A>C
NP_075555.1:p.Asp184Ala
NM_023067.4:c.551A>C
MANE Select
NP_075555.1:p.Asp184Ala
Search 100 bp 5'
Search 100 bp 3'