Canonical Allele Identifier: CA913189426
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 634965
ClinVar RCV Id: RCV000785840
dbSNP Id: rs1559921677
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945621del , CM000665.2:g.138945621del GRCh38
NC_000003.11:g.138664463del , CM000665.1:g.138664463del GRCh37
NC_000003.10:g.140147153del NCBI36
NG_012454.1:g.6521del
NG_029796.1:g.3388del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1103del MANE Select ENSP00000497217.1:p.Gly368AlafsTer?
ENST00000330315.3:c.1103del ENSP00000333188.3:p.Gly368AlafsTer?
NM_023067.3:c.1103del NP_075555.1:p.Gly368AlafsTer?
NM_023067.4:c.1103del MANE Select NP_075555.1:p.Gly368AlafsTer?
Search 100 bp 5'
Search 100 bp 3'