Canonical Allele Identifier: CA2667924891
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945388-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945390del , CM000665.2:g.138945390del GRCh38
NC_000003.11:g.138664232del , CM000665.1:g.138664232del GRCh37
NC_000003.10:g.140146922del NCBI36
NG_012454.1:g.6752del
NG_029796.1:g.3157del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*203del MANE Select ENSP00000497217.1:n.*203del
ENST00000330315.3:c.*203del ENSP00000333188.3:n.*203del
NM_023067.3:c.*203del NP_075555.1:n.*203del
NM_023067.4:c.*203del MANE Select NP_075555.1:n.*203del
Search 100 bp 5'
Search 100 bp 3'