Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38675899A= , CM000685.2:g.38675899A= | GRCh38 |
| NC_000023.10:g.38535153A= , CM000685.1:g.38535153A= | GRCh37 |
| NC_000023.9:g.38420097A= | NCBI36 |
| NG_009160.1:g.119423A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378482.7:c.597+39A= MANE Select | ENSP00000367743.2:n.597+39A= | |
| ENST00000286824.6:c.648+39A= | ENSP00000286824.6:n.648+39A= | |
| ENST00000378482.6:c.597+39A= | ENSP00000367743.2:n.597+39A= | |
| ENST00000419600.3:n.541+39A= | ||
| ENST00000465127.1:c.687+39A= | ENSP00000417050.1:n.687+39A= | |
| ENST00000471410.5:c.*623+39A= | ENSP00000419290.1:n.*623+39A= | |
| ENST00000475216.5:c.*590+39A= | ENSP00000418586.1:n.*590+39A= | |
| NM_004615.3:c.597+39A= | NP_004606.2:n.597+39A= | |
| NM_004615.4:c.597+39A= MANE Select | NP_004606.2:n.597+39A= |