Canonical Allele Identifier: CA448393312
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1332189932
gnomAD v2: 6-1610974-G-A
gnomAD v3: 6-1610739-G-A
gnomAD v4: 6-1610739-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610739G>A , CM000668.2:g.1610739G>A GRCh38
NC_000006.11:g.1610974G>A , CM000668.1:g.1610974G>A GRCh37
NC_000006.10:g.1555973G>A NCBI36
NG_009368.1:g.5294G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.294G>A MANE Select ENSP00000493906.1:p.Lys98=
ENST00000380874.3:c.294G>A ENSP00000370256.2:p.Lys98=
NM_001453.2:c.294G>A NP_001444.2:p.Lys98=
NM_001453.3:c.294G>A MANE Select NP_001444.2:p.Lys98=