Canonical Allele Identifier: CA899581412
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1303533009
MyVariant Identifiers: chr3:g.138664180A>T (hg19) chr3:g.138945338A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945338A>T , CM000665.2:g.138945338A>T GRCh38
NC_000003.11:g.138664180A>T , CM000665.1:g.138664180A>T GRCh37
NC_000003.10:g.140146870A>T NCBI36
NG_012454.1:g.6803T>A
NG_029796.1:g.3105A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*254T>A MANE Select ENSP00000497217.1:n.*254T>A
ENST00000330315.3:c.*254T>A ENSP00000333188.3:n.*254T>A
NM_023067.3:c.*254T>A NP_075555.1:n.*254T>A
NM_023067.4:c.*254T>A MANE Select NP_075555.1:n.*254T>A
Search 100 bp 5'
Search 100 bp 3'