Canonical Allele Identifier: CA362558080
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762516802
gnomAD v3: 6-1610546-G-C
gnomAD v4: 6-1610546-G-C
MyVariant Identifiers: chr6:g.1610781G>C (hg19) chr6:g.1610546G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610546G>C , CM000668.2:g.1610546G>C GRCh38
NC_000006.11:g.1610781G>C , CM000668.1:g.1610781G>C GRCh37
NC_000006.10:g.1555780G>C NCBI36
NG_009368.1:g.5101G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.101G>C MANE Select ENSP00000493906.1:p.Gly34Ala
ENST00000380874.3:c.101G>C ENSP00000370256.2:p.Gly34Ala
NM_001453.2:c.101G>C NP_001444.2:p.Gly34Ala
NM_001453.3:c.101G>C MANE Select NP_001444.2:p.Gly34Ala
Search 100 bp 5'
Search 100 bp 3'