Canonical Allele Identifier: CA2667924830
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945351-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945351G>T , CM000665.2:g.138945351G>T GRCh38
NC_000003.11:g.138664193G>T , CM000665.1:g.138664193G>T GRCh37
NC_000003.10:g.140146883G>T NCBI36
NG_012454.1:g.6790C>A
NG_029796.1:g.3118G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*241C>A MANE Select ENSP00000497217.1:n.*241C>A
ENST00000330315.3:c.*241C>A ENSP00000333188.3:n.*241C>A
NM_023067.3:c.*241C>A NP_075555.1:n.*241C>A
NM_023067.4:c.*241C>A MANE Select NP_075555.1:n.*241C>A
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