Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29388554A= , CM000668.2:g.29388554A= | GRCh38 |
| NC_000006.11:g.29356331A= , CM000668.1:g.29356331A= | GRCh37 |
| NC_000006.10:g.29464310A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377154.1:c.-82-32277T= | ENSP00000366359.1:n.-82-32277T= | |
| XM_011514929.1:c.-82-32277T= | XP_011513231.1:n.-82-32277T= | |
| XM_011514930.1:c.-82-32277T= | XP_011513232.1:n.-82-32277T= | |
| XM_011514931.1:c.-83+17464T= | XP_011513233.1:n.-83+17464T= | |
| XM_011514932.1:c.-82-32277T= | XP_011513234.1:n.-82-32277T= | |
| XM_011514930.2:c.-82-32277T= | XP_011513232.1:n.-82-32277T= | |
| XM_024446562.1:c.-82-32277T= | XP_024302330.1:n.-82-32277T= |