Allele Registry

Canonical Allele Identifier: CA12435398

Gene: CASC15 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr6:g.22017509T>C

GRCh37 chr6:g.22017738T>C

Linked Data - Sequence & Population

gnomAD v2:

6:22017738 T / C

gnomAD v3:

6:22017509 T / C

gnomAD v4:

chr6-22017509-T-C

Joint Max Group AF 0.48532419 (NFE)

Genomes Max Group AF 0.48532419 (NFE)

Linked Data - NCBI & NCI

dbSNP:

1928168

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.22017509T>C , CM000668.2:g.22017509T>C	GRCh38
NC_000006.11:g.22017738T>C , CM000668.1:g.22017738T>C	GRCh37
NC_000006.10:g.22125717T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_015410.1:n.869-2830T>C
NR_015410.2:n.900-2830T>C

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