Canonical Allele Identifier: CA2667924861
Gene: FOXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945371dup , CM000665.2:g.138945371dup GRCh38
NC_000003.11:g.138664213dup , CM000665.1:g.138664213dup GRCh37
NC_000003.10:g.140146903dup NCBI36
NG_012454.1:g.6771dup
NG_029796.1:g.3138dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*222dup MANE Select ENSP00000497217.1:n.*222dup
ENST00000330315.3:c.*222dup ENSP00000333188.3:n.*222dup
NM_023067.3:c.*222dup NP_075555.1:n.*222dup
NM_023067.4:c.*222dup MANE Select NP_075555.1:n.*222dup