Canonical Allele Identifier: CA2667924778
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945319-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945319A>C , CM000665.2:g.138945319A>C GRCh38
NC_000003.11:g.138664161A>C , CM000665.1:g.138664161A>C GRCh37
NC_000003.10:g.140146851A>C NCBI36
NG_012454.1:g.6822T>G
NG_029796.1:g.3086A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*273T>G MANE Select ENSP00000497217.1:n.*273T>G
ENST00000330315.3:c.*273T>G ENSP00000333188.3:n.*273T>G
NM_023067.3:c.*273T>G NP_075555.1:n.*273T>G
NM_023067.4:c.*273T>G MANE Select NP_075555.1:n.*273T>G
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