Canonical Allele Identifier: CA448393298
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610529-G-T
MyVariant Identifiers: chr6:g.1610764G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610529G>T , CM000668.2:g.1610529G>T GRCh38
NC_000006.11:g.1610764G>T , CM000668.1:g.1610764G>T GRCh37
NC_000006.10:g.1555763G>T NCBI36
NG_009368.1:g.5084G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.84G>T MANE Select ENSP00000493906.1:p.Ala28=
ENST00000380874.3:c.84G>T ENSP00000370256.2:p.Ala28=
NM_001453.2:c.84G>T NP_001444.2:p.Ala28=
NM_001453.3:c.84G>T MANE Select NP_001444.2:p.Ala28=
Search 100 bp 5'
Search 100 bp 3'