Canonical Allele Identifier: CA2140882619
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1895025443

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649588G>A , CM000676.2:g.60649588G>A GRCh38
NC_000014.8:g.61116306G>A , CM000676.1:g.61116306G>A GRCh37
NC_000014.7:g.60186059G>A NCBI36
NG_008231.1:g.4850C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2347C>T
ENST00000554986.2:c.42-3011C>T ENSP00000452700.2:n.42-3011C>T
ENST00000555955.3:n.1197+2347C>T