Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154954020A= , CM000685.2:g.154954020A= | GRCh38 |
| NC_000023.10:g.154182295A= , CM000685.1:g.154182295A= | GRCh37 |
| NC_000023.9:g.153835489A= | NCBI36 |
| NG_011403.1:g.73704T= | |
| NG_011403.2:g.73704T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.1775T= MANE Select | ENSP00000353393.4:p.Val592= | |
| ENST00000647125.1:c.*1651T= | ENSP00000496062.1:n.*1651T= | |
| ENST00000360256.8:c.1775T= | ENSP00000353393.4:p.Val592= | |
| NM_000132.3:c.1775T= | NP_000123.1:p.Val592= | |
| XM_011531126.1:c.1670T= | XP_011529428.1:p.Val557= | |
| NM_000132.4:c.1775T= MANE Select | NP_000123.1:p.Val592= |