Canonical Allele Identifier: CA185773149

Gene: CASC11

Linked Data

• dbSNP Id: rs1005582620
• gnomAD v3: 8-127705896-T-C
• gnomAD v4: 8-127705896-T-C
• MyVariant Identifiers: chr8:g.128718141T>C (hg19) ; chr8:g.127705896T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127705896T>C , CM000670.2:g.127705896T>C	GRCh38
NC_000008.10:g.128718141T>C , CM000670.1:g.128718141T>C	GRCh37
NC_000008.9:g.128787323T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_117102.1:n.366-2653A>G