Canonical Allele Identifier: CA2140882800
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1895026886

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649651del , CM000676.2:g.60649651del GRCh38
NC_000014.8:g.61116369del , CM000676.1:g.61116369del GRCh37
NC_000014.7:g.60186122del NCBI36
NG_008231.1:g.4788del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2285del
ENST00000554986.2:c.42-3073del ENSP00000452700.2:n.42-3073del
ENST00000555955.3:n.1197+2285del