Canonical Allele Identifier: CA83969257
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1036640245
gnomAD v3: 3-138945397-T-G
gnomAD v4: 3-138945397-T-G
MyVariant Identifiers: chr3:g.138664239T>G (hg19) chr3:g.138945397T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945397T>G , CM000665.2:g.138945397T>G GRCh38
NC_000003.11:g.138664239T>G , CM000665.1:g.138664239T>G GRCh37
NC_000003.10:g.140146929T>G NCBI36
NG_012454.1:g.6744A>C
NG_029796.1:g.3164T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*195A>C MANE Select ENSP00000497217.1:n.*195A>C
ENST00000330315.3:c.*195A>C ENSP00000333188.3:n.*195A>C
NM_023067.3:c.*195A>C NP_075555.1:n.*195A>C
NM_023067.4:c.*195A>C MANE Select NP_075555.1:n.*195A>C
Search 100 bp 5'
Search 100 bp 3'