Canonical Allele Identifier: CA821645462
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1181818597
gnomAD v4: 6-1610027-C-CA
MyVariant Identifiers: chr6:g.1610262_1610263insA (hg19) chr6:g.1610027_1610028insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610027_1610028insA , CM000668.2:g.1610027_1610028insA GRCh38
NC_000006.11:g.1610262_1610263insA , CM000668.1:g.1610262_1610263insA GRCh37
NC_000006.10:g.1555261_1555262insA NCBI36
NG_009368.1:g.4582_4583insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-419_-418insA MANE Select ENSP00000493906.1:n.-419_-418insA
ENST00000380874.3:c.-419_-418insA ENSP00000370256.2:n.-419_-418insA
NM_001453.3:c.-419_-418insA MANE Select NP_001444.2:n.-419_-418insA
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