Canonical Allele Identifier: CA261723835
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs535243538
gnomAD v2: 14-61116191-A-T
gnomAD v3: 14-60649473-A-T
gnomAD v4: 14-60649473-A-T
MyVariant Identifiers: chr14:g.61116191A>T (hg19) chr14:g.60649473A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649473A>T , CM000676.2:g.60649473A>T GRCh38
NC_000014.8:g.61116191A>T , CM000676.1:g.61116191A>T GRCh37
NC_000014.7:g.60185944A>T NCBI36
NG_008231.1:g.4965T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.-284T>A MANE Select ENSP00000494686.1:n.-284T>A
ENST00000553535.2:n.248+2462T>A
ENST00000554986.2:c.42-2896T>A ENSP00000452700.2:n.42-2896T>A
ENST00000555955.3:n.1197+2462T>A
XM_017021602.2:c.-284T>A XP_016877091.1:n.-284T>A
NM_005982.4:c.-284T>A MANE Select NP_005973.1:n.-284T>A
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