Canonical Allele Identifier: CA707371048
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1247777402
gnomAD v3: 14-60644852-A-T
gnomAD v4: 14-60644852-A-T
MyVariant Identifiers: chr14:g.61111570A>T (hg19) chr14:g.60644852A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60644852A>T , CM000676.2:g.60644852A>T GRCh38
NC_000014.8:g.61111570A>T , CM000676.1:g.61111570A>T GRCh37
NC_000014.7:g.60181323A>T NCBI36
NG_008231.1:g.9586T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.*1431T>A MANE Select ENSP00000494686.1:n.*1431T>A
ENST00000247182.6:c.*1431T>A ENSP00000247182.5:n.*1431T>A
ENST00000554986.2:c.*1431T>A ENSP00000452700.2:n.*1431T>A
NM_005982.3:c.*1431T>A NP_005973.1:n.*1431T>A
XM_017021602.2:c.*1705T>A XP_016877091.1:n.*1705T>A
NM_005982.4:c.*1431T>A MANE Select NP_005973.1:n.*1431T>A
Search 100 bp 5'
Search 100 bp 3'