Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429991T= , CM000663.2:g.68429991T= | GRCh38 |
| NC_000001.10:g.68895674T= , CM000663.1:g.68895674T= | GRCh37 |
| NC_000001.9:g.68668262T= | NCBI36 |
| NG_008472.1:g.24969A= | |
| NG_008472.2:g.24969A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1451-64A= MANE Select | ENSP00000262340.5:n.1451-64A= | |
| ENST00000262340.5:c.1451-64A= | ENSP00000262340.5:n.1451-64A= | |
| NM_000329.2:c.1451-64A= | NP_000320.1:n.1451-64A= | |
| XM_017002027.1:c.1175-64A= | XP_016857516.1:n.1175-64A= | |
| NM_000329.3:c.1451-64A= MANE Select | NP_000320.1:n.1451-64A= |