Allele Registry

Canonical Allele Identifier: CA12264155

Gene: CASC15 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr6:g.22003666A>C

GRCh37 chr6:g.22003895A>C

Linked Data - Sequence & Population

gnomAD v2:

6:22003895 A / C

gnomAD v3:

6:22003666 A / C

gnomAD v4:

chr6-22003666-A-C

Joint Max Group AF 0.56174347 (AFR)

Genomes Max Group AF 0.56174347 (AFR)

Linked Data - NCBI & NCI

dbSNP:

11966463

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.22003666A>C , CM000668.2:g.22003666A>C	GRCh38
NC_000006.11:g.22003895A>C , CM000668.1:g.22003895A>C	GRCh37
NC_000006.10:g.22111874A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_015410.1:n.869-16673A>C
NR_015410.2:n.900-16673A>C

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