Canonical Allele Identifier: CA2140882876
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1895027363
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649673A>T , CM000676.2:g.60649673A>T GRCh38
NC_000014.8:g.61116391A>T , CM000676.1:g.61116391A>T GRCh37
NC_000014.7:g.60186144A>T NCBI36
NG_008231.1:g.4765T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2262T>A
ENST00000554986.2:c.42-3096T>A ENSP00000452700.2:n.42-3096T>A
ENST00000555955.3:n.1197+2262T>A
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