Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48615075A= , CM000681.2:g.48615075A= | GRCh38 |
| NC_000019.9:g.49118332A= , CM000681.1:g.49118332A= | GRCh37 |
| NC_000019.8:g.53810144A= | NCBI36 |
| NG_029867.1:g.785A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263266.4:c.-1526T= MANE Select | ENSP00000263266.2:n.-1526T= | |
| XM_024451561.1:c.-1522T= | XP_024307329.1:n.-1522T= | |
| NM_017708.4:c.-1526T= MANE Select | NP_060178.2:n.-1526T= |