Canonical Allele Identifier: CA354706471
Gene: FOXL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.138665182C>A (hg19) chr3:g.138946340C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946340C>A , CM000665.2:g.138946340C>A GRCh38
NC_000003.11:g.138665182C>A , CM000665.1:g.138665182C>A GRCh37
NC_000003.10:g.140147872C>A NCBI36
NG_012454.1:g.5801G>T
NG_029796.1:g.4107C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.383G>T MANE Select ENSP00000497217.1:p.Trp128Leu
ENST00000330315.3:c.383G>T ENSP00000333188.3:p.Trp128Leu
NM_023067.3:c.383G>T NP_075555.1:p.Trp128Leu
NM_023067.4:c.383G>T MANE Select NP_075555.1:p.Trp128Leu
Search 100 bp 5'
Search 100 bp 3'