Canonical Allele Identifier: CA354700177
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1366646720
gnomAD v2: 3-138664463-C-G
gnomAD v4: 3-138945621-C-G
MyVariant Identifiers: chr3:g.138664463C>G (hg19) chr3:g.138945621C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945621C>G , CM000665.2:g.138945621C>G GRCh38
NC_000003.11:g.138664463C>G , CM000665.1:g.138664463C>G GRCh37
NC_000003.10:g.140147153C>G NCBI36
NG_012454.1:g.6520G>C
NG_029796.1:g.3388C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1102G>C MANE Select ENSP00000497217.1:p.Gly368Arg
ENST00000330315.3:c.1102G>C ENSP00000333188.3:p.Gly368Arg
NM_023067.3:c.1102G>C NP_075555.1:p.Gly368Arg
NM_023067.4:c.1102G>C MANE Select NP_075555.1:p.Gly368Arg
Search 100 bp 5'
Search 100 bp 3'