Canonical Allele Identifier: CA12286586
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs527925646
gnomAD v2: 6-1610198-G-A
gnomAD v3: 6-1609963-G-A
gnomAD v4: 6-1609963-G-A
MyVariant Identifiers: chr6:g.1610198G>A (hg19) chr6:g.1609963G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609963G>A , CM000668.2:g.1609963G>A GRCh38
NC_000006.11:g.1610198G>A , CM000668.1:g.1610198G>A GRCh37
NC_000006.10:g.1555197G>A NCBI36
NG_009368.1:g.4518G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-483G>A MANE Select ENSP00000493906.1:n.-483G>A
NM_001453.3:c.-483G>A MANE Select NP_001444.2:n.-483G>A
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