Canonical Allele Identifier: CA2140883114
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1895029221

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649779C>G , CM000676.2:g.60649779C>G GRCh38
NC_000014.8:g.61116497C>G , CM000676.1:g.61116497C>G GRCh37
NC_000014.7:g.60186250C>G NCBI36
NG_008231.1:g.4659G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2156G>C
ENST00000554986.2:c.42-3202G>C ENSP00000452700.2:n.42-3202G>C
ENST00000555955.3:n.1197+2156G>C