Canonical Allele Identifier: CA133388515
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1000853772
MyVariant Identifiers: chr6:g.1610205A>G (hg19) chr6:g.1609970A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609970A>G , CM000668.2:g.1609970A>G GRCh38
NC_000006.11:g.1610205A>G , CM000668.1:g.1610205A>G GRCh37
NC_000006.10:g.1555204A>G NCBI36
NG_009368.1:g.4525A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-476A>G MANE Select ENSP00000493906.1:n.-476A>G
NM_001453.3:c.-476A>G MANE Select NP_001444.2:n.-476A>G
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