Canonical Allele Identifier: CA448393306
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610736-G-A
MyVariant Identifiers: chr6:g.1610971G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610736G>A , CM000668.2:g.1610736G>A GRCh38
NC_000006.11:g.1610971G>A , CM000668.1:g.1610971G>A GRCh37
NC_000006.10:g.1555970G>A NCBI36
NG_009368.1:g.5291G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.291G>A MANE Select ENSP00000493906.1:p.Lys97=
ENST00000380874.3:c.291G>A ENSP00000370256.2:p.Lys97=
NM_001453.2:c.291G>A NP_001444.2:p.Lys97=
NM_001453.3:c.291G>A MANE Select NP_001444.2:p.Lys97=
Search 100 bp 5'
Search 100 bp 3'