Canonical Allele Identifier: CA362558426
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610707A>G , CM000668.2:g.1610707A>G GRCh38
NC_000006.11:g.1610942A>G , CM000668.1:g.1610942A>G GRCh37
NC_000006.10:g.1555941A>G NCBI36
NG_009368.1:g.5262A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.262A>G MANE Select ENSP00000493906.1:p.Thr88Ala
ENST00000380874.3:c.262A>G ENSP00000370256.2:p.Thr88Ala
NM_001453.2:c.262A>G NP_001444.2:p.Thr88Ala
NM_001453.3:c.262A>G MANE Select NP_001444.2:p.Thr88Ala