Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.65979586G= , CM000673.2:g.65979586G= | GRCh38 |
| NC_000011.9:g.65747057G= , CM000673.1:g.65747057G= | GRCh37 |
| NC_000011.8:g.65503633G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005146.5:c.*556G= MANE Select | NP_005137.1:n.*556G= |
| ENST00000312397.10:c.*556G= MANE Select | ENSP00000310448.5:n.*556G= |
| NM_005146.4:c.*556G= | NP_005137.1:n.*556G= |
| ENST00000312397.9:c.*556G= | ENSP00000310448.5:n.*556G= |