Canonical Allele Identifier: CA362558790
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610871-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610871C>G , CM000668.2:g.1610871C>G GRCh38
NC_000006.11:g.1611106C>G , CM000668.1:g.1611106C>G GRCh37
NC_000006.10:g.1556105C>G NCBI36
NG_009368.1:g.5426C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.426C>G MANE Select ENSP00000493906.1:p.Asp142Glu
ENST00000380874.3:c.426C>G ENSP00000370256.2:p.Asp142Glu
NM_001453.2:c.426C>G NP_001444.2:p.Asp142Glu
NM_001453.3:c.426C>G MANE Select NP_001444.2:p.Asp142Glu