Canonical Allele Identifier: CA2140882387
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649503T= , CM000676.2:g.60649503T= GRCh38
NC_000014.8:g.61116221T= , CM000676.1:g.61116221T= GRCh37
NC_000014.7:g.60185974T= NCBI36
NG_008231.1:g.4935A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2432A=
ENST00000554986.2:c.42-2926A= ENSP00000452700.2:n.42-2926A=
ENST00000555955.3:n.1197+2432A=