Canonical Allele Identifier: CA185773134

Gene: CASC11

Linked Data

• dbSNP Id: rs186808211
• gnomAD v2: 8-128717980-A-T
• gnomAD v3: 8-127705735-A-T
• gnomAD v4: 8-127705735-A-T
• MyVariant Identifiers: chr8:g.128717980A>T (hg19) ; chr8:g.127705735A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127705735A>T , CM000670.2:g.127705735A>T	GRCh38
NC_000008.10:g.128717980A>T , CM000670.1:g.128717980A>T	GRCh37
NC_000008.9:g.128787162A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_117102.1:n.366-2492T>A