Canonical Allele Identifier: CA1085285015
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762581406
gnomAD v3: 6-1612864-T-C
gnomAD v4: 6-1612864-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612864T>C , CM000668.2:g.1612864T>C GRCh38
NC_000006.11:g.1613099T>C , CM000668.1:g.1613099T>C GRCh37
NC_000006.10:g.1558098T>C NCBI36
NG_009368.1:g.7419T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*757T>C MANE Select ENSP00000493906.1:n.*757T>C
ENST00000380874.3:c.*757T>C ENSP00000370256.2:n.*757T>C
NM_001453.2:c.2419T>C NP_001444.2:n.2419T>C
NM_001453.3:c.*757T>C MANE Select NP_001444.2:n.*757T>C
Search 100 bp 5'
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