Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.112830582A= , CM000664.2:g.112830582A= | GRCh38 |
| NC_000002.11:g.113588159A= , CM000664.1:g.113588159A= | GRCh37 |
| NC_000002.10:g.113304630A= | NCBI36 |
| NG_008851.1:g.11198T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263341.7:c.598-9T= MANE Select | ENSP00000263341.2:n.598-9T= | |
| ENST00000263341.6:c.598-9T= | ENSP00000263341.2:n.598-9T= | |
| ENST00000491056.5:n.1405-9T= | ||
| NM_000576.2:c.598-9T= | NP_000567.1:n.598-9T= | |
| XM_006712496.1:c.364-9T= | XP_006712559.1:n.364-9T= | |
| XM_017003988.2:c.505-9T= | XP_016859477.1:n.505-9T= | |
| NM_000576.3:c.598-9T= MANE Select | NP_000567.1:n.598-9T= |