Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28768751A= , CM000676.2:g.28768751A= | GRCh38 |
| NC_000014.8:g.29237957A= , CM000676.1:g.29237957A= | GRCh37 |
| NC_000014.7:g.28307708A= | NCBI36 |
| NG_009367.1:g.6671A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706482.1:c.*2A= | ENSP00000516406.1:n.*2A= | |
| ENST00000313071.7:c.*2A= MANE Select | ENSP00000339004.3:n.*2A= | |
| ENST00000313071.6:c.*2A= | ENSP00000339004.3:n.*2A= | |
| NM_005249.4:c.*2A= | NP_005240.3:n.*2A= | |
| NM_005249.5:c.*2A= MANE Select | NP_005240.3:n.*2A= |