Canonical Allele Identifier: CA362558663
Gene: FOXC1 HGNC NCBI

Linked Data

COSMIC: COSM1075690
MyVariant Identifiers: chr6:g.1611048A>C (hg19) chr6:g.1610813A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610813A>C , CM000668.2:g.1610813A>C GRCh38
NC_000006.11:g.1611048A>C , CM000668.1:g.1611048A>C GRCh37
NC_000006.10:g.1556047A>C NCBI36
NG_009368.1:g.5368A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.368A>C MANE Select ENSP00000493906.1:p.Gln123Pro
ENST00000380874.3:c.368A>C ENSP00000370256.2:p.Gln123Pro
NM_001453.2:c.368A>C NP_001444.2:p.Gln123Pro
NM_001453.3:c.368A>C MANE Select NP_001444.2:p.Gln123Pro
Search 100 bp 5'
Search 100 bp 3'