Canonical Allele Identifier: CA261723927
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1026358263
MyVariant Identifiers: chr14:g.60649557G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649557G>A , CM000676.2:g.60649557G>A GRCh38
NC_000014.8:g.61116275G>A , CM000676.1:g.61116275G>A GRCh37
NC_000014.7:g.60186028G>A NCBI36
NG_008231.1:g.4881C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2378C>T
ENST00000554986.2:c.42-2980C>T ENSP00000452700.2:n.42-2980C>T
ENST00000555955.3:n.1197+2378C>T