Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680089A= , CM000663.2:g.186680089A= | GRCh38 |
| NC_000001.10:g.186649221A= , CM000663.1:g.186649221A= | GRCh37 |
| NC_000001.9:g.184915844A= | NCBI36 |
| NG_028206.2:g.5339T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000963.4:c.52+150T= MANE Select | NP_000954.1:n.52+150T= |
| ENST00000367468.10:c.52+150T= MANE Select | ENSP00000356438.5:n.52+150T= |
| NM_000963.3:c.52+150T= | NP_000954.1:n.52+150T= |
| ENST00000367468.9:c.52+150T= | ENSP00000356438.5:n.52+150T= |
| ENST00000490885.6:n.185+150T= | |
| ENST00000559627.1:c.52+150T= | ENSP00000454130.1:n.52+150T= |
| ENST00000559800.1:n.185+150T= | |
| ENST00000680451.1:c.52+150T= | ENSP00000506242.1:n.52+150T= |
| ENST00000681605.1:c.52+150T= | ENSP00000504900.1:n.52+150T= |