Canonical Allele Identifier: CA2677061056
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612705-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612705G>T , CM000668.2:g.1612705G>T GRCh38
NC_000006.11:g.1612940G>T , CM000668.1:g.1612940G>T GRCh37
NC_000006.10:g.1557939G>T NCBI36
NG_009368.1:g.7260G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*598G>T MANE Select ENSP00000493906.1:n.*598G>T
ENST00000380874.3:c.*598G>T ENSP00000370256.2:n.*598G>T
NM_001453.2:c.2260G>T NP_001444.2:n.2260G>T
NM_001453.3:c.*598G>T MANE Select NP_001444.2:n.*598G>T
Search 100 bp 5'
Search 100 bp 3'