Canonical Allele Identifier: CA1605821872
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762500242
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609968A>C , CM000668.2:g.1609968A>C GRCh38
NC_000006.11:g.1610203A>C , CM000668.1:g.1610203A>C GRCh37
NC_000006.10:g.1555202A>C NCBI36
NG_009368.1:g.4523A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-478A>C MANE Select ENSP00000493906.1:n.-478A>C
NM_001453.3:c.-478A>C MANE Select NP_001444.2:n.-478A>C
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