Canonical Allele Identifier: CA1605821832
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762499272
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609929_1609931del , CM000668.2:g.1609929_1609931del GRCh38
NC_000006.11:g.1610164_1610166del , CM000668.1:g.1610164_1610166del GRCh37
NC_000006.10:g.1555163_1555165del NCBI36
NG_009368.1:g.4484_4486del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-517_-515del MANE Select ENSP00000493906.1:n.-517_-515del
NM_001453.3:c.-517_-515del MANE Select NP_001444.2:n.-517_-515del
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Search 100 bp 3'