Canonical Allele Identifier: CA448393613
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762524381
MyVariant Identifiers: chr6:g.1611097G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610862G>A , CM000668.2:g.1610862G>A GRCh38
NC_000006.11:g.1611097G>A , CM000668.1:g.1611097G>A GRCh37
NC_000006.10:g.1556096G>A NCBI36
NG_009368.1:g.5417G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.417G>A MANE Select ENSP00000493906.1:p.Val139=
ENST00000380874.3:c.417G>A ENSP00000370256.2:p.Val139=
NM_001453.2:c.417G>A NP_001444.2:p.Val139=
NM_001453.3:c.417G>A MANE Select NP_001444.2:p.Val139=