Canonical Allele Identifier: CA354707779

Gene: FOXL2

Linked Data

• MyVariant Identifiers: chr3:g.138665413G>T (hg19) ; chr3:g.138946571G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138946571G>T , CM000665.2:g.138946571G>T	GRCh38
NC_000003.11:g.138665413G>T , CM000665.1:g.138665413G>T	GRCh37
NC_000003.10:g.140148103G>T	NCBI36
NG_012454.1:g.5570C>A
NG_029796.1:g.4338G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.152C>A MANE Select	ENSP00000497217.1:p.Pro51Gln
ENST00000330315.3:c.152C>A	ENSP00000333188.3:p.Pro51Gln
NM_023067.3:c.152C>A	NP_075555.1:p.Pro51Gln
NM_023067.4:c.152C>A MANE Select	NP_075555.1:p.Pro51Gln