Canonical Allele Identifier: CA436093956
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1380242545
gnomAD v2: 3-138664560-G-C
gnomAD v3: 3-138945718-G-C
gnomAD v4: 3-138945718-G-C
MyVariant Identifiers: chr3:g.138664560G>C (hg19) chr3:g.138945718G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945718G>C , CM000665.2:g.138945718G>C GRCh38
NC_000003.11:g.138664560G>C , CM000665.1:g.138664560G>C GRCh37
NC_000003.10:g.140147250G>C NCBI36
NG_012454.1:g.6423C>G
NG_029796.1:g.3485G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1005C>G MANE Select ENSP00000497217.1:p.Pro335=
ENST00000330315.3:c.1005C>G ENSP00000333188.3:p.Pro335=
NM_023067.3:c.1005C>G NP_075555.1:p.Pro335=
NM_023067.4:c.1005C>G MANE Select NP_075555.1:p.Pro335=
Search 100 bp 5'
Search 100 bp 3'