Canonical Allele Identifier: CA185773142

Gene: CASC11

Linked Data

• dbSNP Id: rs950005928
• gnomAD v2: 8-128718098-T-C
• gnomAD v3: 8-127705853-T-C
• gnomAD v4: 8-127705853-T-C
• MyVariant Identifiers: chr8:g.128718098T>C (hg19) ; chr8:g.127705853T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127705853T>C , CM000670.2:g.127705853T>C	GRCh38
NC_000008.10:g.128718098T>C , CM000670.1:g.128718098T>C	GRCh37
NC_000008.9:g.128787280T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_117102.1:n.366-2610A>G