Canonical Allele Identifier: CA362558344
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610670-C-G
MyVariant Identifiers: chr6:g.1610905C>G (hg19) chr6:g.1610670C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610670C>G , CM000668.2:g.1610670C>G GRCh38
NC_000006.11:g.1610905C>G , CM000668.1:g.1610905C>G GRCh37
NC_000006.10:g.1555904C>G NCBI36
NG_009368.1:g.5225C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.225C>G MANE Select ENSP00000493906.1:p.Asp75Glu
ENST00000380874.3:c.225C>G ENSP00000370256.2:p.Asp75Glu
NM_001453.2:c.225C>G NP_001444.2:p.Asp75Glu
NM_001453.3:c.225C>G MANE Select NP_001444.2:p.Asp75Glu
Search 100 bp 5'
Search 100 bp 3'