Canonical Allele Identifier: CA448393313
Gene: FOXC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.1610773G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610538G>C , CM000668.2:g.1610538G>C GRCh38
NC_000006.11:g.1610773G>C , CM000668.1:g.1610773G>C GRCh37
NC_000006.10:g.1555772G>C NCBI36
NG_009368.1:g.5093G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.93G>C MANE Select ENSP00000493906.1:p.Ala31=
ENST00000380874.3:c.93G>C ENSP00000370256.2:p.Ala31=
NM_001453.2:c.93G>C NP_001444.2:p.Ala31=
NM_001453.3:c.93G>C MANE Select NP_001444.2:p.Ala31=
Search 100 bp 5'
Search 100 bp 3'