Canonical Allele Identifier: CA436094211
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107743414
gnomAD v4: 3-138945868-C-G
MyVariant Identifiers: chr3:g.138664710C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945868C>G , CM000665.2:g.138945868C>G GRCh38
NC_000003.11:g.138664710C>G , CM000665.1:g.138664710C>G GRCh37
NC_000003.10:g.140147400C>G NCBI36
NG_012454.1:g.6273G>C
NG_029796.1:g.3635C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.855G>C MANE Select ENSP00000497217.1:p.Pro285=
ENST00000330315.3:c.855G>C ENSP00000333188.3:p.Pro285=
NM_023067.3:c.855G>C NP_075555.1:p.Pro285=
NM_023067.4:c.855G>C MANE Select NP_075555.1:p.Pro285=
Search 100 bp 5'
Search 100 bp 3'