Canonical Allele Identifier: CA136301852
Gene: CASC15 HGNC NCBI
NBAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1006199224
gnomAD v3: 6-22139593-T-C
gnomAD v4: 6-22139593-T-C
MyVariant Identifiers: chr6:g.22139822T>C (hg19) chr6:g.22139593T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.22139593T>C , CM000668.2:g.22139593T>C GRCh38
NC_000006.11:g.22139822T>C , CM000668.1:g.22139822T>C GRCh37
NC_000006.10:g.22247801T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015410.1:n.1391+28673T>C (CASC15)
NR_034143.1:n.228-2924A>G (NBAT1)
NR_015410.2:n.1422+28673T>C (CASC15)
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