Canonical Allele Identifier: CA2517296986
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610322A>T , CM000668.2:g.1610322A>T GRCh38
NC_000006.11:g.1610557A>T , CM000668.1:g.1610557A>T GRCh37
NC_000006.10:g.1555556A>T NCBI36
NG_009368.1:g.4877A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-124A>T MANE Select ENSP00000493906.1:n.-124A>T
ENST00000380874.3:c.-124A>T ENSP00000370256.2:n.-124A>T
NM_001453.3:c.-124A>T MANE Select NP_001444.2:n.-124A>T