Canonical Allele Identifier: CA10654882
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369912
ClinVar RCV Id: RCV000408857 RCV002523842
dbSNP Id: rs1057516161
gnomAD v2: 3-138664988-T-TG
gnomAD v4: 3-138946146-T-TG
MyVariant Identifiers: chr3:g.138664989dupG (hg19) chr3:g.138664989_138664990insG (hg19) chr3:g.138664988_138664989insG (hg19) chr3:g.138946147dupG (hg38) chr3:g.138946147_138946148insG (hg38) chr3:g.138946146_138946147insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946152dup , CM000665.2:g.138946152dup GRCh38
NC_000003.11:g.138664994dup , CM000665.1:g.138664994dup GRCh37
NC_000003.10:g.140147684dup NCBI36
NG_012454.1:g.5994dup
NG_029796.1:g.3919dup

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.576dup MANE Select ENSP00000497217.1:p.Lys193GlnfsTer?
ENST00000330315.3:c.576dup ENSP00000333188.3:p.Lys193GlnfsTer?
NM_023067.3:c.576dup NP_075555.1:p.Lys193GlnfsTer?
NM_023067.4:c.576dup MANE Select NP_075555.1:p.Lys193GlnfsTer?
Search 100 bp 5'
Search 100 bp 3'