Canonical Allele Identifier: CA546892488

Gene: FOXL2

Linked Data

• dbSNP Id: rs769794895
• gnomAD v2: 3-138664412-T-G
• gnomAD v4: 3-138945570-T-G
• MyVariant Identifiers: chr3:g.138664412T>G (hg19) ; chr3:g.138945570T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945570T>G , CM000665.2:g.138945570T>G	GRCh38
NC_000003.11:g.138664412T>G , CM000665.1:g.138664412T>G	GRCh37
NC_000003.10:g.140147102T>G	NCBI36
NG_012454.1:g.6571A>C
NG_029796.1:g.3337T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*22A>C MANE Select	ENSP00000497217.1:n.*22A>C
ENST00000330315.3:c.*22A>C	ENSP00000333188.3:n.*22A>C
NM_023067.3:c.*22A>C	NP_075555.1:n.*22A>C
NM_023067.4:c.*22A>C MANE Select	NP_075555.1:n.*22A>C