Canonical Allele Identifier: CA354700241
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1237990062
gnomAD v2: 3-138664472-T-C
gnomAD v3: 3-138945630-T-C
gnomAD v4: 3-138945630-T-C
MyVariant Identifiers: chr3:g.138664472T>C (hg19) chr3:g.138945630T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945630T>C , CM000665.2:g.138945630T>C GRCh38
NC_000003.11:g.138664472T>C , CM000665.1:g.138664472T>C GRCh37
NC_000003.10:g.140147162T>C NCBI36
NG_012454.1:g.6511A>G
NG_029796.1:g.3397T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1093A>G MANE Select ENSP00000497217.1:p.Ser365Gly
ENST00000330315.3:c.1093A>G ENSP00000333188.3:p.Ser365Gly
NM_023067.3:c.1093A>G NP_075555.1:p.Ser365Gly
NM_023067.4:c.1093A>G MANE Select NP_075555.1:p.Ser365Gly
Search 100 bp 5'
Search 100 bp 3'