Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.119930207T= , CM000685.2:g.119930207T= | GRCh38 |
| NC_000023.10:g.119064170T= , CM000685.1:g.119064170T= | GRCh37 |
| NC_000023.9:g.118948198T= | NCBI36 |
| NG_021260.1:g.18566A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371410.5:c.924-42A= MANE Select | ENSP00000360464.3:n.924-42A= | |
| ENST00000652253.1:c.920-42A= | ||
| ENST00000371410.4:c.924-42A= | ENSP00000360464.3:n.924-42A= | |
| ENST00000477789.5:n.1852-42A= | ||
| ENST00000482407.1:n.723-42A= | ||
| NM_024528.3:c.924-42A= | NP_078804.2:n.924-42A= | |
| XM_017029842.1:c.627-42A= | XP_016885331.1:n.627-42A= | |
| NM_024528.4:c.924-42A= MANE Select | NP_078804.2:n.924-42A= |