Canonical Allele Identifier: CA546892491
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs199498438
gnomAD v2: 3-138664422-T-G
gnomAD v4: 3-138945580-T-G
MyVariant Identifiers: chr3:g.138664422T>G (hg19) chr3:g.138945580T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945580T>G , CM000665.2:g.138945580T>G GRCh38
NC_000003.11:g.138664422T>G , CM000665.1:g.138664422T>G GRCh37
NC_000003.10:g.140147112T>G NCBI36
NG_012454.1:g.6561A>C
NG_029796.1:g.3347T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*12A>C MANE Select ENSP00000497217.1:n.*12A>C
ENST00000330315.3:c.*12A>C ENSP00000333188.3:n.*12A>C
NM_023067.3:c.*12A>C NP_075555.1:n.*12A>C
NM_023067.4:c.*12A>C MANE Select NP_075555.1:n.*12A>C
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