Canonical Allele Identifier: CA10654879
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369915
dbSNP Id: rs1057516164

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946111C>T , CM000665.2:g.138946111C>T GRCh38
NC_000003.11:g.138664953C>T , CM000665.1:g.138664953C>T GRCh37
NC_000003.10:g.140147643C>T NCBI36
NG_012454.1:g.6030G>A
NG_029796.1:g.3878C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.612G>A MANE Select ENSP00000497217.1:p.Trp204Ter
ENST00000330315.3:c.612G>A ENSP00000333188.3:p.Trp204Ter
NM_023067.3:c.612G>A NP_075555.1:p.Trp204Ter
NM_023067.4:c.612G>A MANE Select NP_075555.1:p.Trp204Ter