Canonical Allele Identifier: CA821650007
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1352759512
gnomAD v4: 6-1612534-G-T
MyVariant Identifiers: chr6:g.1612769G>T (hg19) chr6:g.1612534G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612534G>T , CM000668.2:g.1612534G>T GRCh38
NC_000006.11:g.1612769G>T , CM000668.1:g.1612769G>T GRCh37
NC_000006.10:g.1557768G>T NCBI36
NG_009368.1:g.7089G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*427G>T MANE Select ENSP00000493906.1:n.*427G>T
ENST00000380874.3:c.*427G>T ENSP00000370256.2:n.*427G>T
NM_001453.2:c.2089G>T NP_001444.2:n.2089G>T
NM_001453.3:c.*427G>T MANE Select NP_001444.2:n.*427G>T
Search 100 bp 5'
Search 100 bp 3'