Canonical Allele Identifier: CA436094236
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945886-G-C
MyVariant Identifiers: chr3:g.138664728G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945886G>C , CM000665.2:g.138945886G>C GRCh38
NC_000003.11:g.138664728G>C , CM000665.1:g.138664728G>C GRCh37
NC_000003.10:g.140147418G>C NCBI36
NG_012454.1:g.6255C>G
NG_029796.1:g.3653G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.837C>G MANE Select ENSP00000497217.1:p.Gly279=
ENST00000330315.3:c.837C>G ENSP00000333188.3:p.Gly279=
NM_023067.3:c.837C>G NP_075555.1:p.Gly279=
NM_023067.4:c.837C>G MANE Select NP_075555.1:p.Gly279=
Search 100 bp 5'
Search 100 bp 3'