Canonical Allele Identifier: CA565018147
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1213026019
gnomAD v2: 6-1610152-T-C
gnomAD v3: 6-1609917-T-C
gnomAD v4: 6-1609917-T-C
MyVariant Identifiers: chr6:g.1610152T>C (hg19) chr6:g.1609917T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609917T>C , CM000668.2:g.1609917T>C GRCh38
NC_000006.11:g.1610152T>C , CM000668.1:g.1610152T>C GRCh37
NC_000006.10:g.1555151T>C NCBI36
NG_009368.1:g.4472T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-529T>C MANE Select ENSP00000493906.1:n.-529T>C
NM_001453.3:c.-529T>C MANE Select NP_001444.2:n.-529T>C
Search 100 bp 5'
Search 100 bp 3'