Canonical Allele Identifier: CA2667924807
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945336-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945336G>T , CM000665.2:g.138945336G>T GRCh38
NC_000003.11:g.138664178G>T , CM000665.1:g.138664178G>T GRCh37
NC_000003.10:g.140146868G>T NCBI36
NG_012454.1:g.6805C>A
NG_029796.1:g.3103G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*256C>A MANE Select ENSP00000497217.1:n.*256C>A
ENST00000330315.3:c.*256C>A ENSP00000333188.3:n.*256C>A
NM_023067.3:c.*256C>A NP_075555.1:n.*256C>A
NM_023067.4:c.*256C>A MANE Select NP_075555.1:n.*256C>A
Search 100 bp 5'
Search 100 bp 3'