Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.75769680A= , CM000669.2:g.75769680A= | GRCh38 |
| NC_000007.13:g.75398998A= , CM000669.1:g.75398998A= | GRCh37 |
| NC_000007.12:g.75236934A= | NCBI36 |
| NG_015989.1:g.25067T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000005180.9:c.*13T= MANE Select | ENSP00000005180.4:n.*13T= | |
| ENST00000005180.8:c.*13T= | ENSP00000005180.4:n.*13T= | |
| ENST00000394905.2:c.*13T= | ENSP00000378365.2:n.*13T= | |
| NM_006072.4:c.*13T= | NP_006063.1:n.*13T= | |
| XM_017011671.1:c.*13T= | XP_016867160.1:n.*13T= | |
| XM_017011672.1:c.*13T= | XP_016867161.1:n.*13T= | |
| NM_001371936.1:c.*13T= | NP_001358865.1:n.*13T= | |
| NM_001371938.1:c.*13T= MANE Select | NP_001358867.1:n.*13T= |