Canonical Allele Identifier: CA1605822226
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762512865
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610364A>G , CM000668.2:g.1610364A>G GRCh38
NC_000006.11:g.1610599A>G , CM000668.1:g.1610599A>G GRCh37
NC_000006.10:g.1555598A>G NCBI36
NG_009368.1:g.4919A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-82A>G MANE Select ENSP00000493906.1:n.-82A>G
ENST00000380874.3:c.-82A>G ENSP00000370256.2:n.-82A>G
NM_001453.3:c.-82A>G MANE Select NP_001444.2:n.-82A>G
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