Canonical Allele Identifier: CA362559278
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1611092C>G , CM000668.2:g.1611092C>G GRCh38
NC_000006.11:g.1611327C>G , CM000668.1:g.1611327C>G GRCh37
NC_000006.10:g.1556326C>G NCBI36
NG_009368.1:g.5647C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.647C>G MANE Select ENSP00000493906.1:p.Pro216Arg
ENST00000380874.3:c.647C>G ENSP00000370256.2:p.Pro216Arg
NM_001453.2:c.647C>G NP_001444.2:p.Pro216Arg
NM_001453.3:c.647C>G MANE Select NP_001444.2:p.Pro216Arg