Canonical Allele Identifier: CA436093683
Gene: FOXL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.138664437G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945595G>T , CM000665.2:g.138945595G>T GRCh38
NC_000003.11:g.138664437G>T , CM000665.1:g.138664437G>T GRCh37
NC_000003.10:g.140147127G>T NCBI36
NG_012454.1:g.6546C>A
NG_029796.1:g.3362G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1128C>A MANE Select ENSP00000497217.1:p.Leu376=
ENST00000330315.3:c.1128C>A ENSP00000333188.3:p.Leu376=
NM_023067.3:c.1128C>A NP_075555.1:p.Leu376=
NM_023067.4:c.1128C>A MANE Select NP_075555.1:p.Leu376=
Search 100 bp 5'
Search 100 bp 3'