Canonical Allele Identifier: CA821650056
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1313521976
MyVariant Identifiers: chr6:g.1612875G>A (hg19) chr6:g.1612640G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612640G>A , CM000668.2:g.1612640G>A GRCh38
NC_000006.11:g.1612875G>A , CM000668.1:g.1612875G>A GRCh37
NC_000006.10:g.1557874G>A NCBI36
NG_009368.1:g.7195G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*533G>A MANE Select ENSP00000493906.1:n.*533G>A
ENST00000380874.3:c.*533G>A ENSP00000370256.2:n.*533G>A
NM_001453.2:c.2195G>A NP_001444.2:n.2195G>A
NM_001453.3:c.*533G>A MANE Select NP_001444.2:n.*533G>A
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