Canonical Allele Identifier: CA354706957
Gene: FOXL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.138665269T>G (hg19) chr3:g.138946427T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946427T>G , CM000665.2:g.138946427T>G GRCh38
NC_000003.11:g.138665269T>G , CM000665.1:g.138665269T>G GRCh37
NC_000003.10:g.140147959T>G NCBI36
NG_012454.1:g.5714A>C
NG_029796.1:g.4194T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.296A>C MANE Select ENSP00000497217.1:p.Gln99Pro
ENST00000330315.3:c.296A>C ENSP00000333188.3:p.Gln99Pro
NM_023067.3:c.296A>C NP_075555.1:p.Gln99Pro
NM_023067.4:c.296A>C MANE Select NP_075555.1:p.Gln99Pro
Search 100 bp 5'
Search 100 bp 3'