Canonical Allele Identifier: CA2667925011
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945489-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945489G>C , CM000665.2:g.138945489G>C GRCh38
NC_000003.11:g.138664331G>C , CM000665.1:g.138664331G>C GRCh37
NC_000003.10:g.140147021G>C NCBI36
NG_012454.1:g.6652C>G
NG_029796.1:g.3256G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*103C>G MANE Select ENSP00000497217.1:n.*103C>G
ENST00000330315.3:c.*103C>G ENSP00000333188.3:n.*103C>G
NM_023067.3:c.*103C>G NP_075555.1:n.*103C>G
NM_023067.4:c.*103C>G MANE Select NP_075555.1:n.*103C>G
Search 100 bp 5'
Search 100 bp 3'