Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31658350A>T , CM000668.2:g.31658350A>T | GRCh38 |
| NC_000006.11:g.31626127A>T , CM000668.1:g.31626127A>T | GRCh37 |
| NC_000006.10:g.31734106A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_021184.4:c.*713T>A (C6orf47) MANE Select | NP_067007.3:n.*713T>A |
| ENST00000375911.2:c.*713T>A (C6orf47) MANE Select | ENSP00000365076.1:n.*713T>A |
| NM_021184.3:c.*713T>A (C6orf47) | NP_067007.3:n.*713T>A |
| ENST00000375911.1:c.*713T>A (C6orf47) | ENSP00000365076.1:n.*713T>A |
| XM_011514895.1:c.-14+1971T>A (BAG6) | XP_011513197.1:n.-14+1971T>A |
| XM_017011279.2:c.-14+1971T>A (BAG6) | XP_016866768.1:n.-14+1971T>A |