Canonical Allele Identifier: CA261724097

Gene: SIX1

Linked Data

• dbSNP Id: rs1045529868
• MyVariant Identifiers: chr14:g.61116383G>T (hg19) ; chr14:g.60649665G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60649665G>T , CM000676.2:g.60649665G>T	GRCh38
NC_000014.8:g.61116383G>T , CM000676.1:g.61116383G>T	GRCh37
NC_000014.7:g.60186136G>T	NCBI36
NG_008231.1:g.4773C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553535.2:n.248+2270C>A
ENST00000554986.2:c.42-3088C>A	ENSP00000452700.2:n.42-3088C>A
ENST00000555955.3:n.1197+2270C>A