Canonical Allele Identifier: CA210680
Gene: FOXL2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 4853
dbSNP Id: rs104893741

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946068G>A , CM000665.2:g.138946068G>A GRCh38
NC_000003.10:g.140147600G>A NCBI36
NC_000003.11:g.138664910G>A , CM000665.1:g.138664910G>A GRCh37
NG_012454.1:g.6073C>T
NG_029796.1:g.3835G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000330315.3:c.655C>T ENSP00000333188.3:p.Gln219Ter
NM_023067.3:c.655C>T NP_075555.1:p.Gln219Ter