Canonical Allele Identifier: CA2537765064
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649678T>C , CM000676.2:g.60649678T>C GRCh38
NC_000014.8:g.61116396T>C , CM000676.1:g.61116396T>C GRCh37
NC_000014.7:g.60186149T>C NCBI36
NG_008231.1:g.4760A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2257A>G
ENST00000554986.2:c.42-3101A>G ENSP00000452700.2:n.42-3101A>G
ENST00000555955.3:n.1197+2257A>G