Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940584A= , CM000678.2:g.67940584A= | GRCh38 |
| NC_000016.9:g.67974487A= , CM000678.1:g.67974487A= | GRCh37 |
| NC_000016.8:g.66531988A= | NCBI36 |
| NG_009778.1:g.8529T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.749-106T= MANE Select | ENSP00000264005.5:n.749-106T= | |
| ENST00000264005.9:c.749-106T= | ENSP00000264005.5:n.749-106T= | |
| ENST00000570369.5:c.156-510T= | ||
| ENST00000570980.1:c.533-106T= | ENSP00000464651.1:n.533-106T= | |
| ENST00000573538.5:c.487-106T= | ENSP00000463220.1:n.487-106T= | |
| NM_000229.1:c.749-106T= | NP_000220.1:n.749-106T= | |
| NM_000229.2:c.749-106T= MANE Select | NP_000220.1:n.749-106T= |