Canonical Allele Identifier: CA2140883048
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649743T= , CM000676.2:g.60649743T= GRCh38
NC_000014.8:g.61116461T= , CM000676.1:g.61116461T= GRCh37
NC_000014.7:g.60186214T= NCBI36
NG_008231.1:g.4695A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2192A=
ENST00000554986.2:c.42-3166A= ENSP00000452700.2:n.42-3166A=
ENST00000555955.3:n.1197+2192A=