Canonical Allele Identifier: CA1605821907
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609999A= , CM000668.2:g.1609999A= GRCh38
NC_000006.11:g.1610234A= , CM000668.1:g.1610234A= GRCh37
NC_000006.10:g.1555233A= NCBI36
NG_009368.1:g.4554A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-447A= MANE Select ENSP00000493906.1:n.-447A=
ENST00000380874.3:c.-447A= ENSP00000370256.2:n.-447A=
NM_001453.3:c.-447A= MANE Select NP_001444.2:n.-447A=