Canonical Allele Identifier: CA566128338
Gene: CASC15 HGNC NCBI

Linked Data

dbSNP Id: rs1187134843
gnomAD v2: 6-22131732-C-T
gnomAD v3: 6-22131503-C-T
gnomAD v4: 6-22131503-C-T
MyVariant Identifiers: chr6:g.22131732C>T (hg19) chr6:g.22131503C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.22131503C>T , CM000668.2:g.22131503C>T GRCh38
NC_000006.11:g.22131732C>T , CM000668.1:g.22131732C>T GRCh37
NC_000006.10:g.22239711C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015410.1:n.1391+20583C>T
NR_015410.2:n.1422+20583C>T
Search 100 bp 5'
Search 100 bp 3'