Canonical Allele Identifier: CA354706881
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946419T>C , CM000665.2:g.138946419T>C GRCh38
NC_000003.11:g.138665261T>C , CM000665.1:g.138665261T>C GRCh37
NC_000003.10:g.140147951T>C NCBI36
NG_012454.1:g.5722A>G
NG_029796.1:g.4186T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.304A>G MANE Select ENSP00000497217.1:p.Ile102Val
ENST00000330315.3:c.304A>G ENSP00000333188.3:p.Ile102Val
NM_023067.3:c.304A>G NP_075555.1:p.Ile102Val
NM_023067.4:c.304A>G MANE Select NP_075555.1:p.Ile102Val