Canonical Allele Identifier: CA1405402064
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs567245375
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945371G>T , CM000665.2:g.138945371G>T GRCh38
NC_000003.11:g.138664213G>T , CM000665.1:g.138664213G>T GRCh37
NC_000003.10:g.140146903G>T NCBI36
NG_012454.1:g.6770C>A
NG_029796.1:g.3138G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*221C>A MANE Select ENSP00000497217.1:n.*221C>A
ENST00000330315.3:c.*221C>A ENSP00000333188.3:n.*221C>A
NM_023067.3:c.*221C>A NP_075555.1:n.*221C>A
NM_023067.4:c.*221C>A MANE Select NP_075555.1:n.*221C>A
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