Canonical Allele Identifier: CA185773122

Gene: CASC11

Linked Data

• dbSNP Id: rs373256471
• gnomAD v2: 8-128717917-C-A
• gnomAD v3: 8-127705672-C-A
• gnomAD v4: 8-127705672-C-A
• MyVariant Identifiers: chr8:g.128717917C>A (hg19) ; chr8:g.127705672C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127705672C>A , CM000670.2:g.127705672C>A	GRCh38
NC_000008.10:g.128717917C>A , CM000670.1:g.128717917C>A	GRCh37
NC_000008.9:g.128787099C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_117102.1:n.366-2429G>T