Canonical Allele Identifier: CA10654908
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369886
ClinVar RCV Id: RCV000408892
dbSNP Id: rs1057516139

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946708G>T , CM000665.2:g.138946708G>T GRCh38
NC_000003.11:g.138665550G>T , CM000665.1:g.138665550G>T GRCh37
NC_000003.10:g.140148240G>T NCBI36
NG_012454.1:g.5433C>A
NG_029796.1:g.4475G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.15C>A MANE Select ENSP00000497217.1:p.Tyr5Ter
ENST00000330315.3:c.15C>A ENSP00000333188.3:p.Tyr5Ter
NM_023067.3:c.15C>A NP_075555.1:p.Tyr5Ter
NM_023067.4:c.15C>A MANE Select NP_075555.1:p.Tyr5Ter