Canonical Allele Identifier: CA448393702
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1319939486
MyVariant Identifiers: chr6:g.1611175C>G (hg19) chr6:g.1610940C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610940C>G , CM000668.2:g.1610940C>G GRCh38
NC_000006.11:g.1611175C>G , CM000668.1:g.1611175C>G GRCh37
NC_000006.10:g.1556174C>G NCBI36
NG_009368.1:g.5495C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.495C>G MANE Select ENSP00000493906.1:p.Gly165=
ENST00000380874.3:c.495C>G ENSP00000370256.2:p.Gly165=
NM_001453.2:c.495C>G NP_001444.2:p.Gly165=
NM_001453.3:c.495C>G MANE Select NP_001444.2:p.Gly165=
Search 100 bp 5'
Search 100 bp 3'