Canonical Allele Identifier: CA2667924822
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945346-G-GC
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945348dup , CM000665.2:g.138945348dup GRCh38
NC_000003.11:g.138664190dup , CM000665.1:g.138664190dup GRCh37
NC_000003.10:g.140146880dup NCBI36
NG_012454.1:g.6794dup
NG_029796.1:g.3115dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*245dup MANE Select ENSP00000497217.1:n.*245dup
ENST00000330315.3:c.*245dup ENSP00000333188.3:n.*245dup
NM_023067.3:c.*245dup NP_075555.1:n.*245dup
NM_023067.4:c.*245dup MANE Select NP_075555.1:n.*245dup
Search 100 bp 5'
Search 100 bp 3'