Canonical Allele Identifier: CA362557987
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610503-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610503G>T , CM000668.2:g.1610503G>T GRCh38
NC_000006.11:g.1610738G>T , CM000668.1:g.1610738G>T GRCh37
NC_000006.10:g.1555737G>T NCBI36
NG_009368.1:g.5058G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.58G>T MANE Select ENSP00000493906.1:p.Gly20Cys
ENST00000380874.3:c.58G>T ENSP00000370256.2:p.Gly20Cys
NM_001453.2:c.58G>T NP_001444.2:p.Gly20Cys
NM_001453.3:c.58G>T MANE Select NP_001444.2:p.Gly20Cys