Canonical Allele Identifier: CA2710888942
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs2113109292
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609925T>C , CM000668.2:g.1609925T>C GRCh38
NC_000006.11:g.1610160T>C , CM000668.1:g.1610160T>C GRCh37
NC_000006.10:g.1555159T>C NCBI36
NG_009368.1:g.4480T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-521T>C MANE Select ENSP00000493906.1:n.-521T>C
NM_001453.3:c.-521T>C MANE Select NP_001444.2:n.-521T>C
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