Canonical Allele Identifier: CA707374741
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1310496419
MyVariant Identifiers: chr14:g.61116413del (hg19) chr14:g.60649695del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649696del , CM000676.2:g.60649696del GRCh38
NC_000014.8:g.61116414del , CM000676.1:g.61116414del GRCh37
NC_000014.7:g.60186167del NCBI36
NG_008231.1:g.4743del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2240del
ENST00000554986.2:c.42-3118del ENSP00000452700.2:n.42-3118del
ENST00000555955.3:n.1197+2240del
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