Canonical Allele Identifier: CA566128810
Gene: CASC15 HGNC NCBI
NBAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1206205758
gnomAD v2: 6-22139936-T-C
gnomAD v3: 6-22139707-T-C
gnomAD v4: 6-22139707-T-C
MyVariant Identifiers: chr6:g.22139936T>C (hg19) chr6:g.22139707T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.22139707T>C , CM000668.2:g.22139707T>C GRCh38
NC_000006.11:g.22139936T>C , CM000668.1:g.22139936T>C GRCh37
NC_000006.10:g.22247915T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015410.1:n.1391+28787T>C (CASC15)
NR_034143.1:n.228-3038A>G (NBAT1)
NR_015410.2:n.1422+28787T>C (CASC15)
Search 100 bp 5'
Search 100 bp 3'