Canonical Allele Identifier: CA354703899
Gene: FOXL2 HGNC NCBI

Linked Data

gnomAD v4: 3-138945981-G-T
MyVariant Identifiers: chr3:g.138664823G>T (hg19) chr3:g.138945981G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945981G>T , CM000665.2:g.138945981G>T GRCh38
NC_000003.11:g.138664823G>T , CM000665.1:g.138664823G>T GRCh37
NC_000003.10:g.140147513G>T NCBI36
NG_012454.1:g.6160C>A
NG_029796.1:g.3748G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.742C>A MANE Select ENSP00000497217.1:p.Leu248Met
ENST00000330315.3:c.742C>A ENSP00000333188.3:p.Leu248Met
NM_023067.3:c.742C>A NP_075555.1:p.Leu248Met
NM_023067.4:c.742C>A MANE Select NP_075555.1:p.Leu248Met
Search 100 bp 5'
Search 100 bp 3'