Canonical Allele Identifier: CA362558463
Gene: FOXC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.1610959C>A (hg19) chr6:g.1610724C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610724C>A , CM000668.2:g.1610724C>A GRCh38
NC_000006.11:g.1610959C>A , CM000668.1:g.1610959C>A GRCh37
NC_000006.10:g.1555958C>A NCBI36
NG_009368.1:g.5279C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.279C>A MANE Select ENSP00000493906.1:p.Asn93Lys
ENST00000380874.3:c.279C>A ENSP00000370256.2:p.Asn93Lys
NM_001453.2:c.279C>A NP_001444.2:p.Asn93Lys
NM_001453.3:c.279C>A MANE Select NP_001444.2:p.Asn93Lys
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