Canonical Allele Identifier: CA362558384
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610687A>T , CM000668.2:g.1610687A>T GRCh38
NC_000006.11:g.1610922A>T , CM000668.1:g.1610922A>T GRCh37
NC_000006.10:g.1555921A>T NCBI36
NG_009368.1:g.5242A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.242A>T MANE Select ENSP00000493906.1:p.Tyr81Phe
ENST00000380874.3:c.242A>T ENSP00000370256.2:p.Tyr81Phe
NM_001453.2:c.242A>T NP_001444.2:p.Tyr81Phe
NM_001453.3:c.242A>T MANE Select NP_001444.2:p.Tyr81Phe