Canonical Allele Identifier: CA136301964
Gene: CASC15 HGNC NCBI
NBAT1 HGNC NCBI

Linked Data

dbSNP Id: rs190688508
gnomAD v2: 6-22139999-G-A
gnomAD v3: 6-22139770-G-A
gnomAD v4: 6-22139770-G-A
MyVariant Identifiers: chr6:g.22139999G>A (hg19) chr6:g.22139770G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.22139770G>A , CM000668.2:g.22139770G>A GRCh38
NC_000006.11:g.22139999G>A , CM000668.1:g.22139999G>A GRCh37
NC_000006.10:g.22247978G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015410.1:n.1391+28850G>A (CASC15)
NR_034143.1:n.228-3101C>T (NBAT1)
NR_015410.2:n.1422+28850G>A (CASC15)
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