Canonical Allele Identifier: CA362558228
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1032706802
MyVariant Identifiers: chr6:g.1610849C>G (hg19) chr6:g.1610614C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610614C>G , CM000668.2:g.1610614C>G GRCh38
NC_000006.11:g.1610849C>G , CM000668.1:g.1610849C>G GRCh37
NC_000006.10:g.1555848C>G NCBI36
NG_009368.1:g.5169C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.169C>G MANE Select ENSP00000493906.1:p.Pro57Ala
ENST00000380874.3:c.169C>G ENSP00000370256.2:p.Pro57Ala
NM_001453.2:c.169C>G NP_001444.2:p.Pro57Ala
NM_001453.3:c.169C>G MANE Select NP_001444.2:p.Pro57Ala
Search 100 bp 5'
Search 100 bp 3'