Canonical Allele Identifier: CA354706841
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946416G>A , CM000665.2:g.138946416G>A GRCh38
NC_000003.11:g.138665258G>A , CM000665.1:g.138665258G>A GRCh37
NC_000003.10:g.140147948G>A NCBI36
NG_012454.1:g.5725C>T
NG_029796.1:g.4183G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.307C>T MANE Select ENSP00000497217.1:p.Arg103Cys
ENST00000330315.3:c.307C>T ENSP00000333188.3:p.Arg103Cys
NM_023067.3:c.307C>T NP_075555.1:p.Arg103Cys
NM_023067.4:c.307C>T MANE Select NP_075555.1:p.Arg103Cys