Canonical Allele Identifier: CA821645449
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1297209971
gnomAD v3: 6-1610024-C-CA
gnomAD v4: 6-1610024-C-CA
MyVariant Identifiers: chr6:g.1610259_1610260insA (hg19) chr6:g.1610024_1610025insA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610024_1610025insA , CM000668.2:g.1610024_1610025insA GRCh38
NC_000006.11:g.1610259_1610260insA , CM000668.1:g.1610259_1610260insA GRCh37
NC_000006.10:g.1555258_1555259insA NCBI36
NG_009368.1:g.4579_4580insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-422_-421insA MANE Select ENSP00000493906.1:n.-422_-421insA
ENST00000380874.3:c.-422_-421insA ENSP00000370256.2:n.-422_-421insA
NM_001453.3:c.-422_-421insA MANE Select NP_001444.2:n.-422_-421insA
Search 100 bp 5'
Search 100 bp 3'