Canonical Allele Identifier: CA362557972
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610497-T-C
MyVariant Identifiers: chr6:g.1610732T>C (hg19) chr6:g.1610497T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610497T>C , CM000668.2:g.1610497T>C GRCh38
NC_000006.11:g.1610732T>C , CM000668.1:g.1610732T>C GRCh37
NC_000006.10:g.1555731T>C NCBI36
NG_009368.1:g.5052T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.52T>C MANE Select ENSP00000493906.1:p.Tyr18His
ENST00000380874.3:c.52T>C ENSP00000370256.2:p.Tyr18His
NM_001453.2:c.52T>C NP_001444.2:p.Tyr18His
NM_001453.3:c.52T>C MANE Select NP_001444.2:p.Tyr18His
Search 100 bp 5'
Search 100 bp 3'