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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA354704651
Gene: FOXL2
HGNC
NCBI
Linked Data
dbSNP Id:
rs2107743834
gnomAD v4:
3-138946083-G-T
MyVariant Identifiers:
chr3:g.138664925G>T (hg19)
chr3:g.138946083G>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.138946083G>T , CM000665.2:g.138946083G>T
GRCh38
NC_000003.11:g.138664925G>T , CM000665.1:g.138664925G>T
GRCh37
NC_000003.10:g.140147615G>T
NCBI36
NG_012454.1:g.6058C>A
NG_029796.1:g.3850G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000648323.1:c.640C>A
MANE Select
ENSP00000497217.1:p.Pro214Thr
ENST00000330315.3:c.640C>A
ENSP00000333188.3:p.Pro214Thr
NM_023067.3:c.640C>A
NP_075555.1:p.Pro214Thr
NM_023067.4:c.640C>A
MANE Select
NP_075555.1:p.Pro214Thr
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