Canonical Allele Identifier: CA2140882552
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1895024836

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649566_60649581dup , CM000676.2:g.60649566_60649581dup GRCh38
NC_000014.8:g.61116284_61116299dup , CM000676.1:g.61116284_61116299dup GRCh37
NC_000014.7:g.60186037_60186052dup NCBI36
NG_008231.1:g.4859_4874dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2356_248+2371dup
ENST00000554986.2:c.42-3002_42-2987dup ENSP00000452700.2:n.42-3002_42-2987dup
ENST00000555955.3:n.1197+2356_1197+2371dup