Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.16255812G= , CM000668.2:g.16255812G= | GRCh38 |
| NC_000006.11:g.16256043G= , CM000668.1:g.16256043G= | GRCh37 |
| NC_000006.10:g.16364022G= | NCBI36 |
| NG_013303.1:g.22233G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259727.5:c.465+1077G= MANE Select | ENSP00000259727.4:n.465+1077G= | |
| ENST00000259727.4:c.465+1077G= | ENSP00000259727.4:n.465+1077G= | |
| NM_006877.3:c.465+1077G= | NP_006868.3:n.465+1077G= | |
| XM_011514508.1:c.465+1077G= | XP_011512810.1:n.465+1077G= | |
| XM_011514508.2:c.465+1077G= | XP_011512810.1:n.465+1077G= | |
| NM_006877.4:c.465+1077G= MANE Select | NP_006868.3:n.465+1077G= |