Canonical Allele Identifier: CA362558697
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610828A>G , CM000668.2:g.1610828A>G GRCh38
NC_000006.11:g.1611063A>G , CM000668.1:g.1611063A>G GRCh37
NC_000006.10:g.1556062A>G NCBI36
NG_009368.1:g.5383A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.383A>G MANE Select ENSP00000493906.1:p.His128Arg
ENST00000380874.3:c.383A>G ENSP00000370256.2:p.His128Arg
NM_001453.2:c.383A>G NP_001444.2:p.His128Arg
NM_001453.3:c.383A>G MANE Select NP_001444.2:p.His128Arg