Canonical Allele Identifier: CA2677061065
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612737-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612737G>T , CM000668.2:g.1612737G>T GRCh38
NC_000006.11:g.1612972G>T , CM000668.1:g.1612972G>T GRCh37
NC_000006.10:g.1557971G>T NCBI36
NG_009368.1:g.7292G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*630G>T MANE Select ENSP00000493906.1:n.*630G>T
ENST00000380874.3:c.*630G>T ENSP00000370256.2:n.*630G>T
NM_001453.2:c.2292G>T NP_001444.2:n.2292G>T
NM_001453.3:c.*630G>T MANE Select NP_001444.2:n.*630G>T