Canonical Allele Identifier: CA2677060950
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612482-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612482G>T , CM000668.2:g.1612482G>T GRCh38
NC_000006.11:g.1612717G>T , CM000668.1:g.1612717G>T GRCh37
NC_000006.10:g.1557716G>T NCBI36
NG_009368.1:g.7037G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*375G>T MANE Select ENSP00000493906.1:n.*375G>T
ENST00000380874.3:c.*375G>T ENSP00000370256.2:n.*375G>T
NM_001453.2:c.2037G>T NP_001444.2:n.2037G>T
NM_001453.3:c.*375G>T MANE Select NP_001444.2:n.*375G>T
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