Canonical Allele Identifier: CA917658573
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1581372987
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609964_1609965del , CM000668.2:g.1609964_1609965del GRCh38
NC_000006.11:g.1610199_1610200del , CM000668.1:g.1610199_1610200del GRCh37
NC_000006.10:g.1555198_1555199del NCBI36
NG_009368.1:g.4519_4520del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-482_-481del MANE Select ENSP00000493906.1:n.-482_-481del
NM_001453.3:c.-482_-481del MANE Select NP_001444.2:n.-482_-481del
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