Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136658982G= , CM000685.2:g.136658982G= | GRCh38 |
| NC_000023.10:g.135741141G= , CM000685.1:g.135741141G= | GRCh37 |
| NC_000023.9:g.135568807G= | NCBI36 |
| NG_007280.1:g.15806G= , LRG_141:g.15806G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*28-57G= | ENSP00000512122.1:n.*28-57G= | |
| ENST00000695725.1:c.157-57G= | ENSP00000512123.1:n.157-57G= | |
| ENST00000695726.1:n.2378-57G= | ||
| ENST00000695729.1:n.3213-57G= | ||
| ENST00000370629.7:c.410-57G= MANE Select | ENSP00000359663.2:n.410-57G= | |
| ENST00000370628.2:c.347-57G= | ENSP00000359662.2:n.347-57G= | |
| ENST00000370629.6:c.410-57G= | ENSP00000359663.2:n.410-57G= | |
| NM_000074.2:c.410-57G= , LRG_141t1:c.410-57G= | NP_000065.1:n.410-57G= | |
| NM_000074.3:c.410-57G= MANE Select | NP_000065.1:n.410-57G= |