Canonical Allele Identifier: CA448393250
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610496-C-T
MyVariant Identifiers: chr6:g.1610731C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610496C>T , CM000668.2:g.1610496C>T GRCh38
NC_000006.11:g.1610731C>T , CM000668.1:g.1610731C>T GRCh37
NC_000006.10:g.1555730C>T NCBI36
NG_009368.1:g.5051C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.51C>T MANE Select ENSP00000493906.1:p.Pro17=
ENST00000380874.3:c.51C>T ENSP00000370256.2:p.Pro17=
NM_001453.2:c.51C>T NP_001444.2:p.Pro17=
NM_001453.3:c.51C>T MANE Select NP_001444.2:p.Pro17=
Search 100 bp 5'
Search 100 bp 3'