Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73640926C= , CM000664.2:g.73640926C= | GRCh38 |
| NC_000002.11:g.73868053C= , CM000664.1:g.73868053C= | GRCh37 |
| NC_000002.10:g.73721561C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272425.4:c.*19G= MANE Select | ENSP00000272425.3:n.*19G= | |
| ENST00000272425.3:c.*19G= | ENSP00000272425.3:n.*19G= | |
| NM_003960.3:c.*19G= | NP_003951.3:n.*19G= | |
| NM_003960.4:c.*19G= MANE Select | NP_003951.3:n.*19G= |