Canonical Allele Identifier: CA821645497
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1259600791
MyVariant Identifiers: chr6:g.1610305_1610306insA (hg19) chr6:g.1610070_1610071insA (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-375dup MANE Select ENSP00000493906.1:n.-375dup
ENST00000380874.3:c.-375dup ENSP00000370256.2:n.-375dup
NM_001453.3:c.-375dup MANE Select NP_001444.2:n.-375dup
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