Canonical Allele Identifier: CA133388436
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs764919124
gnomAD v2: 6-1610155-A-G
gnomAD v3: 6-1609920-A-G
gnomAD v4: 6-1609920-A-G
MyVariant Identifiers: chr6:g.1610155A>G (hg19) chr6:g.1609920A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609920A>G , CM000668.2:g.1609920A>G GRCh38
NC_000006.11:g.1610155A>G , CM000668.1:g.1610155A>G GRCh37
NC_000006.10:g.1555154A>G NCBI36
NG_009368.1:g.4475A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-526A>G MANE Select ENSP00000493906.1:n.-526A>G
NM_001453.3:c.-526A>G MANE Select NP_001444.2:n.-526A>G
Search 100 bp 5'
Search 100 bp 3'