Canonical Allele Identifier: CA2140882947
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649702T= , CM000676.2:g.60649702T= GRCh38
NC_000014.8:g.61116420T= , CM000676.1:g.61116420T= GRCh37
NC_000014.7:g.60186173T= NCBI36
NG_008231.1:g.4736A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2233A=
ENST00000554986.2:c.42-3125A= ENSP00000452700.2:n.42-3125A=
ENST00000555955.3:n.1197+2233A=