Canonical Allele Identifier: CA2140882699
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1895026276

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649620del , CM000676.2:g.60649620del GRCh38
NC_000014.8:g.61116338del , CM000676.1:g.61116338del GRCh37
NC_000014.7:g.60186091del NCBI36
NG_008231.1:g.4820del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2317del
ENST00000554986.2:c.42-3041del ENSP00000452700.2:n.42-3041del
ENST00000555955.3:n.1197+2317del