Canonical Allele Identifier: CA2677060439
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610444-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610444C>G , CM000668.2:g.1610444C>G GRCh38
NC_000006.11:g.1610679C>G , CM000668.1:g.1610679C>G GRCh37
NC_000006.10:g.1555678C>G NCBI36
NG_009368.1:g.4999C>G

Transcript Alleles

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