Canonical Allele Identifier: CA2639731
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs762215312

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945976C>T , CM000665.2:g.138945976C>T GRCh38
NC_000003.11:g.138664818C>T , CM000665.1:g.138664818C>T GRCh37
NC_000003.10:g.140147508C>T NCBI36
NG_012454.1:g.6165G>A
NG_029796.1:g.3743C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.747G>A MANE Select ENSP00000497217.1:p.Ala249=
ENST00000330315.3:c.747G>A ENSP00000333188.3:p.Ala249=
NM_023067.3:c.747G>A NP_075555.1:p.Ala249=
NM_023067.4:c.747G>A MANE Select NP_075555.1:p.Ala249=