Canonical Allele Identifier: CA136296570
Gene: CASC15 HGNC NCBI

Linked Data

dbSNP Id: rs1028134719
gnomAD v2: 6-22132031-G-A
gnomAD v3: 6-22131802-G-A
gnomAD v4: 6-22131802-G-A
MyVariant Identifiers: chr6:g.22132031G>A (hg19) chr6:g.22131802G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.22131802G>A , CM000668.2:g.22131802G>A GRCh38
NC_000006.11:g.22132031G>A , CM000668.1:g.22132031G>A GRCh37
NC_000006.10:g.22240010G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_015410.1:n.1391+20882G>A
NR_015410.2:n.1422+20882G>A
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