Canonical Allele Identifier: CA2667924828
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107742710
gnomAD v4: 3-138945349-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945353del , CM000665.2:g.138945353del GRCh38
NC_000003.11:g.138664195del , CM000665.1:g.138664195del GRCh37
NC_000003.10:g.140146885del NCBI36
NG_012454.1:g.6791del
NG_029796.1:g.3120del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*242del MANE Select ENSP00000497217.1:n.*242del
ENST00000330315.3:c.*242del ENSP00000333188.3:n.*242del
NM_023067.3:c.*242del NP_075555.1:n.*242del
NM_023067.4:c.*242del MANE Select NP_075555.1:n.*242del
Search 100 bp 5'
Search 100 bp 3'