Canonical Allele Identifier: CA354704660

Gene: FOXL2

Linked Data

• MyVariant Identifiers: chr3:g.138664926C>G (hg19) ; chr3:g.138946084C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138946084C>G , CM000665.2:g.138946084C>G	GRCh38
NC_000003.11:g.138664926C>G , CM000665.1:g.138664926C>G	GRCh37
NC_000003.10:g.140147616C>G	NCBI36
NG_012454.1:g.6057G>C
NG_029796.1:g.3851C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000648323.1:c.639G>C MANE Select	ENSP00000497217.1:p.Met213Ile
ENST00000330315.3:c.639G>C	ENSP00000333188.3:p.Met213Ile
NM_023067.3:c.639G>C	NP_075555.1:p.Met213Ile
NM_023067.4:c.639G>C MANE Select	NP_075555.1:p.Met213Ile