Canonical Allele Identifier: CA821650168
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1202055515
gnomAD v3: 6-1612882-G-A
gnomAD v4: 6-1612882-G-A
MyVariant Identifiers: chr6:g.1613117G>A (hg19) chr6:g.1612882G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612882G>A , CM000668.2:g.1612882G>A GRCh38
NC_000006.11:g.1613117G>A , CM000668.1:g.1613117G>A GRCh37
NC_000006.10:g.1558116G>A NCBI36
NG_009368.1:g.7437G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*775G>A MANE Select ENSP00000493906.1:n.*775G>A
ENST00000380874.3:c.*775G>A ENSP00000370256.2:n.*775G>A
NM_001453.2:c.2437G>A NP_001444.2:n.2437G>A
NM_001453.3:c.*775G>A MANE Select NP_001444.2:n.*775G>A
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