Canonical Allele Identifier: CA821645419
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs562673925
gnomAD v3: 6-1610015-GCCC-G
gnomAD v4: 6-1610015-GCCC-G
MyVariant Identifiers: chr6:g.1610251_1610253del (hg19) chr6:g.1610016_1610018del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610027_1610029del , CM000668.2:g.1610027_1610029del GRCh38
NC_000006.11:g.1610262_1610264del , CM000668.1:g.1610262_1610264del GRCh37
NC_000006.10:g.1555261_1555263del NCBI36
NG_009368.1:g.4582_4584del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-419_-417del MANE Select ENSP00000493906.1:n.-419_-417del
ENST00000380874.3:c.-419_-417del ENSP00000370256.2:n.-419_-417del
NM_001453.3:c.-419_-417del MANE Select NP_001444.2:n.-419_-417del
Search 100 bp 5'
Search 100 bp 3'