Canonical Allele Identifier: CA565018163
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1310491021
gnomAD v2: 6-1610226-GCCCGGGCAGGCGGCCGGCGCGCGGCCC-G
gnomAD v3: 6-1609991-GCCCGGGCAGGCGGCCGGCGCGCGGCCC-G
gnomAD v4: 6-1609991-GCCCGGGCAGGCGGCCGGCGCGCGGCCC-G
MyVariant Identifiers: chr6:g.1610227_1610253del (hg19) chr6:g.1609992_1610018del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609995_1610021del , CM000668.2:g.1609995_1610021del GRCh38
NC_000006.11:g.1610230_1610256del , CM000668.1:g.1610230_1610256del GRCh37
NC_000006.10:g.1555229_1555255del NCBI36
NG_009368.1:g.4550_4576del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-451_-425del MANE Select ENSP00000493906.1:n.-451_-425del
ENST00000380874.3:c.-451_-425del ENSP00000370256.2:n.-451_-425del
NM_001453.3:c.-451_-425del MANE Select NP_001444.2:n.-451_-425del
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