Canonical Allele Identifier: CA362558385
Gene: FOXC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.1610923T>A (hg19) chr6:g.1610688T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610688T>A , CM000668.2:g.1610688T>A GRCh38
NC_000006.11:g.1610923T>A , CM000668.1:g.1610923T>A GRCh37
NC_000006.10:g.1555922T>A NCBI36
NG_009368.1:g.5243T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.243T>A MANE Select ENSP00000493906.1:p.Tyr81Ter
ENST00000380874.3:c.243T>A ENSP00000370256.2:p.Tyr81Ter
NM_001453.2:c.243T>A NP_001444.2:p.Tyr81Ter
NM_001453.3:c.243T>A MANE Select NP_001444.2:p.Tyr81Ter
Search 100 bp 5'
Search 100 bp 3'