Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18388955T= , CM000681.2:g.18388955T= | GRCh38 |
| NC_000019.9:g.18499765T= , CM000681.1:g.18499765T= | GRCh37 |
| NC_000019.8:g.18360765T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252809.3:c.*20T= MANE Select | ENSP00000252809.3:n.*20T= | |
| NM_004864.2:c.*20T= | NP_004855.2:n.*20T= | |
| NM_004864.3:c.*20T= | NP_004855.2:n.*20T= | |
| XM_024451789.1:c.*20T= | XP_024307557.1:n.*20T= | |
| NM_004864.4:c.*20T= MANE Select | NP_004855.2:n.*20T= |