Canonical Allele Identifier: CA362558748
Gene: FOXC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.1611085C>G (hg19) chr6:g.1610850C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610850C>G , CM000668.2:g.1610850C>G GRCh38
NC_000006.11:g.1611085C>G , CM000668.1:g.1611085C>G GRCh37
NC_000006.10:g.1556084C>G NCBI36
NG_009368.1:g.5405C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.405C>G MANE Select ENSP00000493906.1:p.Cys135Trp
ENST00000380874.3:c.405C>G ENSP00000370256.2:p.Cys135Trp
NM_001453.2:c.405C>G NP_001444.2:p.Cys135Trp
NM_001453.3:c.405C>G MANE Select NP_001444.2:p.Cys135Trp
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