Canonical Allele Identifier: CA12440265
Gene: CASC15 HGNC NCBI
NBAT1 HGNC NCBI

Linked Data

dbSNP Id: rs140912531
gnomAD v2: 6-22140143-T-G
gnomAD v3: 6-22139914-T-G
gnomAD v4: 6-22139914-T-G
MyVariant Identifiers: chr6:g.22140143T>G (hg19) chr6:g.22139914T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.22139914T>G , CM000668.2:g.22139914T>G GRCh38
NC_000006.11:g.22140143T>G , CM000668.1:g.22140143T>G GRCh37
NC_000006.10:g.22248122T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015410.1:n.1391+28994T>G (CASC15)
NR_034143.1:n.228-3245A>C (NBAT1)
NR_015410.2:n.1422+28994T>G (CASC15)
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