Canonical Allele Identifier: CA362558400
Gene: FOXC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.1610929C>G (hg19) chr6:g.1610694C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610694C>G , CM000668.2:g.1610694C>G GRCh38
NC_000006.11:g.1610929C>G , CM000668.1:g.1610929C>G GRCh37
NC_000006.10:g.1555928C>G NCBI36
NG_009368.1:g.5249C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.249C>G MANE Select ENSP00000493906.1:p.Tyr83Ter
ENST00000380874.3:c.249C>G ENSP00000370256.2:p.Tyr83Ter
NM_001453.2:c.249C>G NP_001444.2:p.Tyr83Ter
NM_001453.3:c.249C>G MANE Select NP_001444.2:p.Tyr83Ter
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