Canonical Allele Identifier: CA362558286
Gene: FOXC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.1610879T>G (hg19) chr6:g.1610644T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610644T>G , CM000668.2:g.1610644T>G GRCh38
NC_000006.11:g.1610879T>G , CM000668.1:g.1610879T>G GRCh37
NC_000006.10:g.1555878T>G NCBI36
NG_009368.1:g.5199T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.199T>G MANE Select ENSP00000493906.1:p.Tyr67Asp
ENST00000380874.3:c.199T>G ENSP00000370256.2:p.Tyr67Asp
NM_001453.2:c.199T>G NP_001444.2:p.Tyr67Asp
NM_001453.3:c.199T>G MANE Select NP_001444.2:p.Tyr67Asp
Search 100 bp 5'
Search 100 bp 3'