Canonical Allele Identifier: CA12886193

Gene: CASC11

Linked Data

• dbSNP Id: rs10094872
• gnomAD v2: 8-128719884-A-T
• gnomAD v3: 8-127707639-A-T
• gnomAD v4: 8-127707639-A-T
• MyVariant Identifiers: chr8:g.128719884A>T (hg19) ; chr8:g.127707639A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127707639A>T , CM000670.2:g.127707639A>T	GRCh38
NC_000008.10:g.128719884A>T , CM000670.1:g.128719884A>T	GRCh37
NC_000008.9:g.128789066A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_117102.1:n.366-4396T>A