Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63832084T= , CM000679.2:g.63832084T= | GRCh38 |
| NC_000017.10:g.61909444T= , CM000679.1:g.61909444T= | GRCh37 |
| NC_000017.9:g.59263176T= | NCBI36 |
| NG_053004.1:g.15908A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000448276.7:c.*854A= MANE Select | ENSP00000392617.2:n.*854A= | |
| ENST00000448276.6:c.*854A= | ENSP00000392617.2:n.*854A= | |
| ENST00000613943.4:c.2339A= | ENSP00000483605.1:n.2339A= | |
| NM_001098426.1:c.*854A= | NP_001091896.1:n.*854A= | |
| XM_005257604.2:c.*854A= | XP_005257661.2:n.*854A= | |
| NM_001330439.1:c.*854A= | NP_001317368.1:n.*854A= | |
| NM_001330440.1:c.*854A= | NP_001317369.1:n.*854A= | |
| NM_001098426.2:c.*854A= MANE Select | NP_001091896.1:n.*854A= | |
| NM_001330440.2:c.*854A= | NP_001317369.1:n.*854A= |