Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94949294A= , CM000672.2:g.94949294A= | GRCh38 |
| NC_000010.10:g.96709051A= , CM000672.1:g.96709051A= | GRCh37 |
| NC_000010.9:g.96699041A= | NCBI36 |
| NG_008385.1:g.15637A= | |
| NG_008385.2:g.16137A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.819+10A= MANE Select | ENSP00000260682.6:n.819+10A= | |
| ENST00000643112.1:c.819+10A= | ENSP00000496202.1:n.819+10A= | |
| ENST00000260682.6:c.819+10A= | ENSP00000260682.6:n.819+10A= | |
| ENST00000473496.1:n.600A= | ||
| NM_000771.3:c.819+10A= | NP_000762.2:n.819+10A= | |
| NM_000771.4:c.819+10A= MANE Select | NP_000762.2:n.819+10A= |