Canonical Allele Identifier: CA436094115
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1364469578
gnomAD v3: 3-138946000-C-G
gnomAD v4: 3-138946000-C-G
MyVariant Identifiers: chr3:g.138664842C>G (hg19) chr3:g.138946000C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946000C>G , CM000665.2:g.138946000C>G GRCh38
NC_000003.11:g.138664842C>G , CM000665.1:g.138664842C>G GRCh37
NC_000003.10:g.140147532C>G NCBI36
NG_012454.1:g.6141G>C
NG_029796.1:g.3767C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.723G>C MANE Select ENSP00000497217.1:p.Ala241=
ENST00000330315.3:c.723G>C ENSP00000333188.3:p.Ala241=
NM_023067.3:c.723G>C NP_075555.1:p.Ala241=
NM_023067.4:c.723G>C MANE Select NP_075555.1:p.Ala241=
Search 100 bp 5'
Search 100 bp 3'