Canonical Allele Identifier: CA448393605
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1379307944
gnomAD v2: 6-1610923-T-C
gnomAD v3: 6-1610688-T-C
gnomAD v4: 6-1610688-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610688T>C , CM000668.2:g.1610688T>C GRCh38
NC_000006.11:g.1610923T>C , CM000668.1:g.1610923T>C GRCh37
NC_000006.10:g.1555922T>C NCBI36
NG_009368.1:g.5243T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.243T>C MANE Select ENSP00000493906.1:p.Tyr81=
ENST00000380874.3:c.243T>C ENSP00000370256.2:p.Tyr81=
NM_001453.2:c.243T>C NP_001444.2:p.Tyr81=
NM_001453.3:c.243T>C MANE Select NP_001444.2:p.Tyr81=