Canonical Allele Identifier: CA546892480
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1294332591
gnomAD v2: 3-138664282-GA-G
gnomAD v3: 3-138945440-GA-G
gnomAD v4: 3-138945440-GA-G
MyVariant Identifiers: chr3:g.138664283del (hg19) chr3:g.138945441del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945445del , CM000665.2:g.138945445del GRCh38
NC_000003.11:g.138664287del , CM000665.1:g.138664287del GRCh37
NC_000003.10:g.140146977del NCBI36
NG_012454.1:g.6700del
NG_029796.1:g.3212del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*151del MANE Select ENSP00000497217.1:n.*151del
ENST00000330315.3:c.*151del ENSP00000333188.3:n.*151del
NM_023067.3:c.*151del NP_075555.1:n.*151del
NM_023067.4:c.*151del MANE Select NP_075555.1:n.*151del
Search 100 bp 5'
Search 100 bp 3'