Canonical Allele Identifier: CA2667924676
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945270-G-GA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945270_138945271insA , CM000665.2:g.138945270_138945271insA GRCh38
NC_000003.11:g.138664112_138664113insA , CM000665.1:g.138664112_138664113insA GRCh37
NC_000003.10:g.140146802_140146803insA NCBI36
NG_012454.1:g.6870_6871insT
NG_029796.1:g.3037_3038insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*321_*322insT MANE Select ENSP00000497217.1:n.*321_*322insT
ENST00000330315.3:c.*321_*322insT ENSP00000333188.3:n.*321_*322insT
NM_023067.3:c.*321_*322insT NP_075555.1:n.*321_*322insT
NM_023067.4:c.*321_*322insT MANE Select NP_075555.1:n.*321_*322insT
Search 100 bp 5'
Search 100 bp 3'