Canonical Allele Identifier: CA899582539
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1306984236
gnomAD v4: 3-138946024-GGCTGCAGCCGCAGCTGCTGCAGCC-G
MyVariant Identifiers: chr3:g.138664867_138664890del (hg19) chr3:g.138946025_138946048del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946030_138946053del , CM000665.2:g.138946030_138946053del GRCh38
NC_000003.11:g.138664872_138664895del , CM000665.1:g.138664872_138664895del GRCh37
NC_000003.10:g.140147562_140147585del NCBI36
NG_012454.1:g.6093_6116del
NG_029796.1:g.3797_3820del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.675_698del MANE Select ENSP00000497217.1:p.Ala226_Ala233del
ENST00000330315.3:c.675_698del ENSP00000333188.3:p.Ala226_Ala233del
NM_023067.3:c.675_698del NP_075555.1:p.Ala226_Ala233del
NM_023067.4:c.675_698del MANE Select NP_075555.1:p.Ala226_Ala233del
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