Canonical Allele Identifier: CA210687
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4863
dbSNP Id: rs28937884

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946472A>C , CM000665.2:g.138946472A>C GRCh38
NC_000003.11:g.138665314A>C , CM000665.1:g.138665314A>C GRCh37
NC_000003.10:g.140148004A>C NCBI36
NG_012454.1:g.5669T>G
NG_029796.1:g.4239A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.251T>G MANE Select ENSP00000497217.1:p.Ile84Ser
ENST00000330315.3:c.251T>G ENSP00000333188.3:p.Ile84Ser
NM_023067.3:c.251T>G NP_075555.1:p.Ile84Ser
NM_023067.4:c.251T>G MANE Select NP_075555.1:p.Ile84Ser