Canonical Allele Identifier: CA707374757
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1444229105
gnomAD v3: 14-60649713-T-C
gnomAD v4: 14-60649713-T-C
MyVariant Identifiers: chr14:g.61116431T>C (hg19) chr14:g.60649713T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649713T>C , CM000676.2:g.60649713T>C GRCh38
NC_000014.8:g.61116431T>C , CM000676.1:g.61116431T>C GRCh37
NC_000014.7:g.60186184T>C NCBI36
NG_008231.1:g.4725A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2222A>G
ENST00000554986.2:c.42-3136A>G ENSP00000452700.2:n.42-3136A>G
ENST00000555955.3:n.1197+2222A>G
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