Canonical Allele Identifier: CA2625129262
Gene: SIX1 HGNC NCBI

Linked Data

gnomAD v4: 14-60649503-T-A
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Genomic Alleles

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

Transcript Alleles

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