Canonical Allele Identifier: CA362558093
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762516939
gnomAD v4: 6-1610554-T-C
MyVariant Identifiers: chr6:g.1610789T>C (hg19) chr6:g.1610554T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610554T>C , CM000668.2:g.1610554T>C GRCh38
NC_000006.11:g.1610789T>C , CM000668.1:g.1610789T>C GRCh37
NC_000006.10:g.1555788T>C NCBI36
NG_009368.1:g.5109T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.109T>C MANE Select ENSP00000493906.1:p.Tyr37His
ENST00000380874.3:c.109T>C ENSP00000370256.2:p.Tyr37His
NM_001453.2:c.109T>C NP_001444.2:p.Tyr37His
NM_001453.3:c.109T>C MANE Select NP_001444.2:p.Tyr37His
Search 100 bp 5'
Search 100 bp 3'