Linked Data
gnomAD v2:
6-22140093-A-ATTTT
gnomAD v3:
6-22139864-A-ATTTT
gnomAD v4:
6-22139864-A-ATTTT
MyVariant Identifiers:
chr6:g.22140094_22140095insTTTT (hg19)
chr6:g.22139865_22139866insTTTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.22139872_22139875dup , CM000668.2:g.22139872_22139875dup | GRCh38 |
| NC_000006.11:g.22140101_22140104dup , CM000668.1:g.22140101_22140104dup | GRCh37 |
| NC_000006.10:g.22248080_22248083dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_015410.1:n.1391+28952_1391+28955dup (CASC15) | ||
| NR_034143.1:n.228-3199_228-3196dup (NBAT1) | ||
| NR_015410.2:n.1422+28952_1422+28955dup (CASC15) |