Canonical Allele Identifier: CA136296427
Gene: CASC15 HGNC NCBI

Linked Data

dbSNP Id: rs749128073
MyVariant Identifiers: chr6:g.22131861G>A (hg19) chr6:g.22131632G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.22131632G>A , CM000668.2:g.22131632G>A GRCh38
NC_000006.11:g.22131861G>A , CM000668.1:g.22131861G>A GRCh37
NC_000006.10:g.22239840G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015410.1:n.1391+20712G>A
NR_015410.2:n.1422+20712G>A
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