Canonical Allele Identifier: CA566128398

Gene: CASC15

Linked Data

• dbSNP Id: rs1304209252
• gnomAD v2: 6-22131970-A-T
• gnomAD v3: 6-22131741-A-T
• gnomAD v4: 6-22131741-A-T
• MyVariant Identifiers: chr6:g.22131970A>T (hg19) ; chr6:g.22131741A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.22131741A>T , CM000668.2:g.22131741A>T	GRCh38
NC_000006.11:g.22131970A>T , CM000668.1:g.22131970A>T	GRCh37
NC_000006.10:g.22239949A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_015410.1:n.1391+20821A>T
NR_015410.2:n.1422+20821A>T