Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151822631C= , CM000667.2:g.151822631C= | GRCh38 |
| NC_000005.9:g.151202192C= , CM000667.1:g.151202192C= | GRCh37 |
| NC_000005.8:g.151182385C= | NCBI36 |
| NG_011764.1:g.107206G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274576.9:c.*42G= MANE Select | ENSP00000274576.5:n.*42G= | |
| ENST00000274576.8:c.*42G= | ENSP00000274576.4:n.*42G= | |
| ENST00000455880.2:c.*42G= | ENSP00000411593.2:n.*42G= | |
| ENST00000462581.6:c.*1150G= | ENSP00000430595.1:n.*1150G= | |
| NM_000171.3:c.*42G= | NP_000162.2:n.*42G= | |
| NM_001146040.1:c.*42G= | NP_001139512.1:n.*42G= | |
| NM_001292000.1:c.*42G= | NP_001278929.1:n.*42G= | |
| NM_000171.4:c.*42G= MANE Select | NP_000162.2:n.*42G= | |
| NM_001146040.2:c.*42G= | NP_001139512.1:n.*42G= | |
| NM_001292000.2:c.*42G= | NP_001278929.1:n.*42G= |