Canonical Allele Identifier: CA821645496
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1356393275
gnomAD v3: 6-1610068-CAG-C
gnomAD v4: 6-1610068-CAG-C
MyVariant Identifiers: chr6:g.1610304_1610305del (hg19) chr6:g.1610069_1610070del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610071_1610072del , CM000668.2:g.1610071_1610072del GRCh38
NC_000006.11:g.1610306_1610307del , CM000668.1:g.1610306_1610307del GRCh37
NC_000006.10:g.1555305_1555306del NCBI36
NG_009368.1:g.4626_4627del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-375_-374del MANE Select ENSP00000493906.1:n.-375_-374del
ENST00000380874.3:c.-375_-374del ENSP00000370256.2:n.-375_-374del
NM_001453.3:c.-375_-374del MANE Select NP_001444.2:n.-375_-374del
Search 100 bp 5'
Search 100 bp 3'