Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71124368C= , CM000664.2:g.71124368C= | GRCh38 |
| NC_000002.11:g.71351498C= , CM000664.1:g.71351498C= | GRCh37 |
| NC_000002.10:g.71205006C= | NCBI36 |
| NG_008977.1:g.10897G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244217.6:c.216G= MANE Select | ENSP00000244217.5:p.Gln72= | |
| ENST00000244217.5:c.216G= | ENSP00000244217.5:p.Gln72= | |
| ENST00000413592.5:c.84G= | ENSP00000391140.1:p.Gln28= | |
| ENST00000486135.1:c.-70G= | ENSP00000441569.1:n.-70G= | |
| ENST00000494660.6:c.-70G= | ENSP00000437361.1:n.-70G= | |
| NM_032601.3:c.216G= | NP_115990.3:p.Gln72= | |
| XM_005264613.2:c.216G= | XP_005264670.1:p.Gln72= | |
| XR_939729.1:n.285G= | ||
| XR_939729.2:n.285G= | ||
| NM_032601.4:c.216G= MANE Select | NP_115990.3:p.Gln72= |