Canonical Allele Identifier: CA821645529
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1229581698
gnomAD v4: 6-1610138-TC-T
MyVariant Identifiers: chr6:g.1610374del (hg19) chr6:g.1610139del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610143del , CM000668.2:g.1610143del GRCh38
NC_000006.11:g.1610378del , CM000668.1:g.1610378del GRCh37
NC_000006.10:g.1555377del NCBI36
NG_009368.1:g.4698del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-303del MANE Select ENSP00000493906.1:n.-303del
ENST00000380874.3:c.-303del ENSP00000370256.2:n.-303del
NM_001453.3:c.-303del MANE Select NP_001444.2:n.-303del
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Search 100 bp 3'