Canonical Allele Identifier: CA1405402013
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs1935926782
gnomAD v4: 3-138945309-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945309C>A , CM000665.2:g.138945309C>A GRCh38
NC_000003.11:g.138664151C>A , CM000665.1:g.138664151C>A GRCh37
NC_000003.10:g.140146841C>A NCBI36
NG_012454.1:g.6832G>T
NG_029796.1:g.3076C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*283G>T MANE Select ENSP00000497217.1:n.*283G>T
ENST00000330315.3:c.*283G>T ENSP00000333188.3:n.*283G>T
NM_023067.3:c.*283G>T NP_075555.1:n.*283G>T
NM_023067.4:c.*283G>T MANE Select NP_075555.1:n.*283G>T
Search 100 bp 5'
Search 100 bp 3'