Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.106033494T>C , CM000685.2:g.106033494T>C | GRCh38 |
| NC_000023.10:g.105277485T>C , CM000685.1:g.105277485T>C | GRCh37 |
| NC_000023.9:g.105164141T>C | NCBI36 |
| NG_021252.1:g.10234A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372563.2:c.*6A>G MANE Select | ENSP00000361644.1:n.*6A>G | |
| ENST00000327674.8:c.*6A>G | ENSP00000329374.4:n.*6A>G | |
| ENST00000372563.1:c.*6A>G | ENSP00000361644.1:n.*6A>G | |
| NM_000354.5:c.*6A>G | NP_000345.2:n.*6A>G | |
| XM_006724683.1:c.*6A>G | XP_006724746.1:n.*6A>G | |
| XM_005262180.4:c.*199A>G | XP_005262237.1:n.*199A>G | |
| XM_006724683.2:c.*6A>G | XP_006724746.1:n.*6A>G | |
| NM_000354.6:c.*6A>G MANE Select | NP_000345.2:n.*6A>G |