Canonical Allele Identifier: CA2677061063
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612730-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612730G>T , CM000668.2:g.1612730G>T GRCh38
NC_000006.11:g.1612965G>T , CM000668.1:g.1612965G>T GRCh37
NC_000006.10:g.1557964G>T NCBI36
NG_009368.1:g.7285G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*623G>T MANE Select ENSP00000493906.1:n.*623G>T
ENST00000380874.3:c.*623G>T ENSP00000370256.2:n.*623G>T
NM_001453.2:c.2285G>T NP_001444.2:n.2285G>T
NM_001453.3:c.*623G>T MANE Select NP_001444.2:n.*623G>T