Canonical Allele Identifier: CA354708187
Gene: FOXL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.138665479C>A (hg19) chr3:g.138946637C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946637C>A , CM000665.2:g.138946637C>A GRCh38
NC_000003.11:g.138665479C>A , CM000665.1:g.138665479C>A GRCh37
NC_000003.10:g.140148169C>A NCBI36
NG_012454.1:g.5504G>T
NG_029796.1:g.4404C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.86G>T MANE Select ENSP00000497217.1:p.Gly29Val
ENST00000330315.3:c.86G>T ENSP00000333188.3:p.Gly29Val
NM_023067.3:c.86G>T NP_075555.1:p.Gly29Val
NM_023067.4:c.86G>T MANE Select NP_075555.1:p.Gly29Val
Search 100 bp 5'
Search 100 bp 3'