Canonical Allele Identifier: CA2677060988
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612534-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612534G>A , CM000668.2:g.1612534G>A GRCh38
NC_000006.11:g.1612769G>A , CM000668.1:g.1612769G>A GRCh37
NC_000006.10:g.1557768G>A NCBI36
NG_009368.1:g.7089G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*427G>A MANE Select ENSP00000493906.1:n.*427G>A
ENST00000380874.3:c.*427G>A ENSP00000370256.2:n.*427G>A
NM_001453.2:c.2089G>A NP_001444.2:n.2089G>A
NM_001453.3:c.*427G>A MANE Select NP_001444.2:n.*427G>A
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