Canonical Allele Identifier: CA354707775
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107744951

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946571G>A , CM000665.2:g.138946571G>A GRCh38
NC_000003.11:g.138665413G>A , CM000665.1:g.138665413G>A GRCh37
NC_000003.10:g.140148103G>A NCBI36
NG_012454.1:g.5570C>T
NG_029796.1:g.4338G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.152C>T MANE Select ENSP00000497217.1:p.Pro51Leu
ENST00000330315.3:c.152C>T ENSP00000333188.3:p.Pro51Leu
NM_023067.3:c.152C>T NP_075555.1:p.Pro51Leu
NM_023067.4:c.152C>T MANE Select NP_075555.1:p.Pro51Leu