Canonical Allele Identifier: CA2667924745
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945297-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945297T>G , CM000665.2:g.138945297T>G GRCh38
NC_000003.11:g.138664139T>G , CM000665.1:g.138664139T>G GRCh37
NC_000003.10:g.140146829T>G NCBI36
NG_012454.1:g.6844A>C
NG_029796.1:g.3064T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*295A>C MANE Select ENSP00000497217.1:n.*295A>C
ENST00000330315.3:c.*295A>C ENSP00000333188.3:n.*295A>C
NM_023067.3:c.*295A>C NP_075555.1:n.*295A>C
NM_023067.4:c.*295A>C MANE Select NP_075555.1:n.*295A>C
Search 100 bp 5'
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