Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94941712T= , CM000672.2:g.94941712T= | GRCh38 |
| NC_000010.10:g.96701469T= , CM000672.1:g.96701469T= | GRCh37 |
| NC_000010.9:g.96691459T= | NCBI36 |
| NG_008385.1:g.8055T= | |
| NG_008385.2:g.8555T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.169-146T= MANE Select | ENSP00000260682.6:n.169-146T= | |
| ENST00000643112.1:c.169-146T= | ENSP00000496202.1:n.169-146T= | |
| ENST00000645207.1:n.176T= | ||
| ENST00000260682.6:c.169-146T= | ENSP00000260682.6:n.169-146T= | |
| ENST00000461906.1:n.194-146T= | ||
| NM_000771.3:c.169-146T= | NP_000762.2:n.169-146T= | |
| NM_000771.4:c.169-146T= MANE Select | NP_000762.2:n.169-146T= |