Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154928568T= , CM000685.2:g.154928568T= | GRCh38 |
| NC_000023.10:g.154156843T= , CM000685.1:g.154156843T= | GRCh37 |
| NC_000023.9:g.153810037T= | NCBI36 |
| NG_011403.1:g.99156A= | |
| NG_011403.2:g.99156A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.5219+3A= MANE Select | ENSP00000353393.4:n.5219+3A= | |
| ENST00000360256.8:c.5219+3A= | ENSP00000353393.4:n.5219+3A= | |
| NM_000132.3:c.5219+3A= | NP_000123.1:n.5219+3A= | |
| XM_011531126.1:c.5114+3A= | XP_011529428.1:n.5114+3A= | |
| NM_000132.4:c.5219+3A= MANE Select | NP_000123.1:n.5219+3A= |