Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154953962T= , CM000685.2:g.154953962T= | GRCh38 |
| NC_000023.10:g.154182237T= , CM000685.1:g.154182237T= | GRCh37 |
| NC_000023.9:g.153835431T= | NCBI36 |
| NG_011403.1:g.73762A= | |
| NG_011403.2:g.73762A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.1833A= MANE Select | ENSP00000353393.4:p.Gln611= | |
| ENST00000647125.1:c.*1709A= | ENSP00000496062.1:n.*1709A= | |
| ENST00000360256.8:c.1833A= | ENSP00000353393.4:p.Gln611= | |
| NM_000132.3:c.1833A= | NP_000123.1:p.Gln611= | |
| XM_011531126.1:c.1728A= | XP_011529428.1:p.Gln576= | |
| NM_000132.4:c.1833A= MANE Select | NP_000123.1:p.Gln611= |