Canonical Allele Identifier: CA2667924645
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945263-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945263T>G , CM000665.2:g.138945263T>G GRCh38
NC_000003.11:g.138664105T>G , CM000665.1:g.138664105T>G GRCh37
NC_000003.10:g.140146795T>G NCBI36
NG_012454.1:g.6878A>C
NG_029796.1:g.3030T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*329A>C MANE Select ENSP00000497217.1:n.*329A>C
ENST00000330315.3:c.*329A>C ENSP00000333188.3:n.*329A>C
NM_023067.3:c.*329A>C NP_075555.1:n.*329A>C
NM_023067.4:c.*329A>C MANE Select NP_075555.1:n.*329A>C
Search 100 bp 5'
Search 100 bp 3'