Canonical Allele Identifier: CA821645378
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1042949375
gnomAD v3: 6-1609955-G-T
gnomAD v4: 6-1609955-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609955G>T , CM000668.2:g.1609955G>T GRCh38
NC_000006.11:g.1610190G>T , CM000668.1:g.1610190G>T GRCh37
NC_000006.10:g.1555189G>T NCBI36
NG_009368.1:g.4510G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-491G>T MANE Select ENSP00000493906.1:n.-491G>T
NM_001453.3:c.-491G>T MANE Select NP_001444.2:n.-491G>T