Canonical Allele Identifier: CA83970185
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs997480684
gnomAD v2: 3-138665120-TG-T
gnomAD v3: 3-138946278-TG-T
gnomAD v4: 3-138946278-TG-T
MyVariant Identifiers: chr3:g.138665121del (hg19) chr3:g.138946279del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946279del , CM000665.2:g.138946279del GRCh38
NC_000003.11:g.138665121del , CM000665.1:g.138665121del GRCh37
NC_000003.10:g.140147811del NCBI36
NG_012454.1:g.5862del
NG_029796.1:g.4046del

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.444del MANE Select ENSP00000497217.1:p.Met149Ter
ENST00000330315.3:c.444del ENSP00000333188.3:p.Met149Ter
NM_023067.3:c.444del NP_075555.1:p.Met149Ter
NM_023067.4:c.444del MANE Select NP_075555.1:p.Met149Ter
Search 100 bp 5'
Search 100 bp 3'