Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155427885T= , CM000668.2:g.155427885T= | GRCh38 |
| NC_000006.11:g.155749019T= , CM000668.1:g.155749019T= | GRCh37 |
| NC_000006.10:g.155790711T= | NCBI36 |
| NG_011995.1:g.33019A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000159060.3:c.1145+909A= MANE Select | ENSP00000159060.2:n.1145+909A= | |
| ENST00000159060.2:c.1145+909A= | ENSP00000159060.2:n.1145+909A= | |
| NM_015718.2:c.1145+909A= | NP_056533.1:n.1145+909A= | |
| NM_015718.3:c.1145+909A= MANE Select | NP_056533.1:n.1145+909A= |