Canonical Allele Identifier: CA2677061127
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612933-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612933G>C , CM000668.2:g.1612933G>C GRCh38
NC_000006.11:g.1613168G>C , CM000668.1:g.1613168G>C GRCh37
NC_000006.10:g.1558167G>C NCBI36
NG_009368.1:g.7488G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*826G>C MANE Select ENSP00000493906.1:n.*826G>C
ENST00000380874.3:c.*826G>C ENSP00000370256.2:n.*826G>C
NM_001453.2:c.2488G>C NP_001444.2:n.2488G>C
NM_001453.3:c.*826G>C MANE Select NP_001444.2:n.*826G>C
Search 100 bp 5'
Search 100 bp 3'