Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218893180G= , CM000664.2:g.218893180G= | GRCh38 |
| NC_000002.11:g.219757902G= , CM000664.1:g.219757902G= | GRCh37 |
| NC_000002.10:g.219466146G= | NCBI36 |
| NG_012179.1:g.17648G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.1163G= MANE Select | ENSP00000258411.3:p.Arg388= | |
| ENST00000258411.7:c.1163G= | ENSP00000258411.3:p.Arg388= | |
| NM_025216.2:c.1163G= | NP_079492.2:p.Arg388= | |
| XM_011511928.1:c.1112G= | XP_011510230.1:p.Arg371= | |
| XM_011511929.1:c.1067G= | XP_011510231.1:p.Arg356= | |
| XM_011511930.1:c.783G= | XP_011510232.1:p.Ala261= | |
| XM_011511929.2:c.1067G= | XP_011510231.1:p.Arg356= | |
| NM_025216.3:c.1163G= MANE Select | NP_079492.2:p.Arg388= |