Canonical Allele Identifier: CA2667924951
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945439-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945439C>A , CM000665.2:g.138945439C>A GRCh38
NC_000003.11:g.138664281C>A , CM000665.1:g.138664281C>A GRCh37
NC_000003.10:g.140146971C>A NCBI36
NG_012454.1:g.6702G>T
NG_029796.1:g.3206C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*153G>T MANE Select ENSP00000497217.1:n.*153G>T
ENST00000330315.3:c.*153G>T ENSP00000333188.3:n.*153G>T
NM_023067.3:c.*153G>T NP_075555.1:n.*153G>T
NM_023067.4:c.*153G>T MANE Select NP_075555.1:n.*153G>T
Search 100 bp 5'
Search 100 bp 3'