Canonical Allele Identifier: CA2140883040
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649740A= , CM000676.2:g.60649740A= GRCh38
NC_000014.8:g.61116458A= , CM000676.1:g.61116458A= GRCh37
NC_000014.7:g.60186211A= NCBI36
NG_008231.1:g.4698T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2195T=
ENST00000554986.2:c.42-3163T= ENSP00000452700.2:n.42-3163T=
ENST00000555955.3:n.1197+2195T=