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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:
CA238720
Gene: FOXC1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
193206
ClinVar RCV Id:
RCV000173253
RCV002517662
dbSNP Id:
rs141798688
ExAC:
6:1610959 C / T
gnomAD v2:
6-1610959-C-T
gnomAD v3:
6-1610724-C-T
gnomAD v4:
6-1610724-C-T
MyVariant Identifiers:
chr6:g.1610959C>T (hg19)
chr6:g.1610724C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.1610724C>T , CM000668.2:g.1610724C>T
GRCh38
NC_000006.11:g.1610959C>T , CM000668.1:g.1610959C>T
GRCh37
NC_000006.10:g.1555958C>T
NCBI36
NG_009368.1:g.5279C>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000645831.2:c.279C>T
MANE Select
ENSP00000493906.1:p.Asn93=
ENST00000380874.3:c.279C>T
ENSP00000370256.2:p.Asn93=
NM_001453.2:c.279C>T
NP_001444.2:p.Asn93=
NM_001453.3:c.279C>T
MANE Select
NP_001444.2:p.Asn93=
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