Canonical Allele Identifier: CA585077685

Gene: CASC11

Linked Data

• dbSNP Id: rs1361056427
• gnomAD v2: 8-128717926-G-T
• gnomAD v3: 8-127705681-G-T
• gnomAD v4: 8-127705681-G-T
• MyVariant Identifiers: chr8:g.128717926G>T (hg19) ; chr8:g.127705681G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127705681G>T , CM000670.2:g.127705681G>T	GRCh38
NC_000008.10:g.128717926G>T , CM000670.1:g.128717926G>T	GRCh37
NC_000008.9:g.128787108G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_117102.1:n.366-2438C>A