Canonical Allele Identifier: CA261724083
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs190628563
gnomAD v2: 14-61116372-C-T
gnomAD v3: 14-60649654-C-T
gnomAD v4: 14-60649654-C-T
MyVariant Identifiers: chr14:g.61116372C>T (hg19) chr14:g.60649654C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649654C>T , CM000676.2:g.60649654C>T GRCh38
NC_000014.8:g.61116372C>T , CM000676.1:g.61116372C>T GRCh37
NC_000014.7:g.60186125C>T NCBI36
NG_008231.1:g.4784G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2281G>A
ENST00000554986.2:c.42-3077G>A ENSP00000452700.2:n.42-3077G>A
ENST00000555955.3:n.1197+2281G>A
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