Canonical Allele Identifier: CA261723919
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs995285354
gnomAD v2: 14-61116258-C-T
gnomAD v3: 14-60649540-C-T
gnomAD v4: 14-60649540-C-T
MyVariant Identifiers: chr14:g.61116258C>T (hg19) chr14:g.60649540C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649540C>T , CM000676.2:g.60649540C>T GRCh38
NC_000014.8:g.61116258C>T , CM000676.1:g.61116258C>T GRCh37
NC_000014.7:g.60186011C>T NCBI36
NG_008231.1:g.4898G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2395G>A
ENST00000554986.2:c.42-2963G>A ENSP00000452700.2:n.42-2963G>A
ENST00000555955.3:n.1197+2395G>A
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