Canonical Allele Identifier: CA2667924738
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945291-TG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945295del , CM000665.2:g.138945295del GRCh38
NC_000003.11:g.138664137del , CM000665.1:g.138664137del GRCh37
NC_000003.10:g.140146827del NCBI36
NG_012454.1:g.6849del
NG_029796.1:g.3062del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*300del MANE Select ENSP00000497217.1:n.*300del
ENST00000330315.3:c.*300del ENSP00000333188.3:n.*300del
NM_023067.3:c.*300del NP_075555.1:n.*300del
NM_023067.4:c.*300del MANE Select NP_075555.1:n.*300del
Search 100 bp 5'
Search 100 bp 3'