Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.35878038G= , CM000667.2:g.35878038G= | GRCh38 |
| NC_000005.9:g.35878140G= , CM000667.1:g.35878140G= | GRCh37 |
| NC_000005.8:g.35913897G= | NCBI36 |
| NG_009567.1:g.26150G= , LRG_74:g.26150G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002185.5:c.*1552G= MANE Select | NP_002176.2:n.*1552G= |
| ENST00000303115.8:c.*1552G= MANE Select | ENSP00000306157.3:n.*1552G= |
| NM_002185.3:c.*1552G= | NP_002176.2:n.*1552G= |
| NM_002185.4:c.*1552G= | NP_002176.2:n.*1552G= |
| NR_120485.1:n.2772G= | |
| NR_120485.2:n.2798G= | |
| NR_120485.3:n.2756G= | |
| ENST00000303115.7:c.*1552G= | ENSP00000306157.3:n.*1552G= |
| XM_005248299.4:c.*2049G= | XP_005248356.1:n.*2049G= |