Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965501G= , CM000670.2:g.37965501G= | GRCh38 |
| NC_000008.10:g.37823019G= , CM000670.1:g.37823019G= | GRCh37 |
| NC_000008.9:g.37942176G= | NCBI36 |
| NG_011936.1:g.6166C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.969C= MANE Select | NP_000016.1:p.Val323= |
| ENST00000345060.5:c.969C= MANE Select | ENSP00000343782.3:p.Val323= |
| NM_000025.2:c.969C= | NP_000016.1:p.Val323= |
| ENST00000345060.4:c.969C= | ENSP00000343782.3:p.Val323= |
| ENST00000520341.1:n.244C= | |
| ENST00000520341.2:n.1097C= | |
| ENST00000614635.1:c.969C= | ENSP00000480325.1:p.Val323= |
| ENST00000647937.1:c.453C= | ENSP00000497740.1:p.Val151= |