Canonical Allele Identifier: CA1605821829
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762499174
gnomAD v3: 6-1609923-G-T
gnomAD v4: 6-1609923-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609923G>T , CM000668.2:g.1609923G>T GRCh38
NC_000006.11:g.1610158G>T , CM000668.1:g.1610158G>T GRCh37
NC_000006.10:g.1555157G>T NCBI36
NG_009368.1:g.4478G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-523G>T MANE Select ENSP00000493906.1:n.-523G>T
NM_001453.3:c.-523G>T MANE Select NP_001444.2:n.-523G>T
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