Canonical Allele Identifier: CA362558374
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610683C>G , CM000668.2:g.1610683C>G GRCh38
NC_000006.11:g.1610918C>G , CM000668.1:g.1610918C>G GRCh37
NC_000006.10:g.1555917C>G NCBI36
NG_009368.1:g.5238C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.238C>G MANE Select ENSP00000493906.1:p.Pro80Ala
ENST00000380874.3:c.238C>G ENSP00000370256.2:p.Pro80Ala
NM_001453.2:c.238C>G NP_001444.2:p.Pro80Ala
NM_001453.3:c.238C>G MANE Select NP_001444.2:p.Pro80Ala