Canonical Allele Identifier: CA10654891
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369903
ClinVar RCV Id: RCV000408889
dbSNP Id: rs1057516154
MyVariant Identifiers: chr3:g.138665250_138665252del (hg19) chr3:g.138946408_138946410del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946410_138946412del , CM000665.2:g.138946410_138946412del GRCh38
NC_000003.11:g.138665252_138665254del , CM000665.1:g.138665252_138665254del GRCh37
NC_000003.10:g.140147942_140147944del NCBI36
NG_012454.1:g.5731_5733del
NG_029796.1:g.4177_4179del

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.313_315del MANE Select ENSP00000497217.1:p.Asn105del
ENST00000330315.3:c.313_315del ENSP00000333188.3:p.Asn105del
NM_023067.3:c.313_315del NP_075555.1:p.Asn105del
NM_023067.4:c.313_315del MANE Select NP_075555.1:p.Asn105del
Search 100 bp 5'
Search 100 bp 3'