Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155427842A= , CM000668.2:g.155427842A= | GRCh38 |
| NC_000006.11:g.155748976A= , CM000668.1:g.155748976A= | GRCh37 |
| NC_000006.10:g.155790668A= | NCBI36 |
| NG_011995.1:g.33062T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000159060.3:c.1145+952T= MANE Select | ENSP00000159060.2:n.1145+952T= | |
| ENST00000159060.2:c.1145+952T= | ENSP00000159060.2:n.1145+952T= | |
| NM_015718.2:c.1145+952T= | NP_056533.1:n.1145+952T= | |
| NM_015718.3:c.1145+952T= MANE Select | NP_056533.1:n.1145+952T= |