Canonical Allele Identifier: CA1605821959
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762503293
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610030del , CM000668.2:g.1610030del GRCh38
NC_000006.11:g.1610265del , CM000668.1:g.1610265del GRCh37
NC_000006.10:g.1555264del NCBI36
NG_009368.1:g.4585del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-416del MANE Select ENSP00000493906.1:n.-416del
ENST00000380874.3:c.-416del ENSP00000370256.2:n.-416del
NM_001453.3:c.-416del MANE Select NP_001444.2:n.-416del
Search 100 bp 5'
Search 100 bp 3'