Canonical Allele Identifier: CA354704120
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946011T>G , CM000665.2:g.138946011T>G GRCh38
NC_000003.11:g.138664853T>G , CM000665.1:g.138664853T>G GRCh37
NC_000003.10:g.140147543T>G NCBI36
NG_012454.1:g.6130A>C
NG_029796.1:g.3778T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.712A>C MANE Select ENSP00000497217.1:p.Ser238Arg
ENST00000330315.3:c.712A>C ENSP00000333188.3:p.Ser238Arg
NM_023067.3:c.712A>C NP_075555.1:p.Ser238Arg
NM_023067.4:c.712A>C MANE Select NP_075555.1:p.Ser238Arg