Canonical Allele Identifier: CA136296494
Gene: CASC15 HGNC NCBI

Linked Data

dbSNP Id: rs894074913
gnomAD v3: 6-22131682-A-G
gnomAD v4: 6-22131682-A-G
MyVariant Identifiers: chr6:g.22131911A>G (hg19) chr6:g.22131682A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.22131682A>G , CM000668.2:g.22131682A>G GRCh38
NC_000006.11:g.22131911A>G , CM000668.1:g.22131911A>G GRCh37
NC_000006.10:g.22239890A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015410.1:n.1391+20762A>G
NR_015410.2:n.1422+20762A>G
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