Canonical Allele Identifier: CA899581401
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1341600580
gnomAD v3: 3-138945315-C-T
gnomAD v4: 3-138945315-C-T
MyVariant Identifiers: chr3:g.138664157C>T (hg19) chr3:g.138945315C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945315C>T , CM000665.2:g.138945315C>T GRCh38
NC_000003.11:g.138664157C>T , CM000665.1:g.138664157C>T GRCh37
NC_000003.10:g.140146847C>T NCBI36
NG_012454.1:g.6826G>A
NG_029796.1:g.3082C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*277G>A MANE Select ENSP00000497217.1:n.*277G>A
ENST00000330315.3:c.*277G>A ENSP00000333188.3:n.*277G>A
NM_023067.3:c.*277G>A NP_075555.1:n.*277G>A
NM_023067.4:c.*277G>A MANE Select NP_075555.1:n.*277G>A
Search 100 bp 5'
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