Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16137994C= , CM000663.2:g.16137994C= | GRCh38 |
| NC_000001.10:g.16464489C= , CM000663.1:g.16464489C= | GRCh37 |
| NC_000001.9:g.16337076C= | NCBI36 |
| NG_021396.1:g.23094G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358432.8:c.1171G= MANE Select | ENSP00000351209.5:p.Gly391= | |
| ENST00000358432.7:c.1171G= | ENSP00000351209.5:p.Gly391= | |
| ENST00000480202.1:n.376G= | ||
| NM_004431.3:c.1171G= | NP_004422.2:p.Gly391= | |
| NM_001329090.1:c.1009G= | NP_001316019.1:p.Gly337= | |
| NM_004431.4:c.1171G= | NP_004422.2:p.Gly391= | |
| XM_017000537.1:c.1171G= | XP_016856026.1:p.Gly391= | |
| NM_004431.5:c.1171G= MANE Select | NP_004422.2:p.Gly391= | |
| NM_001329090.2:c.1009G= | NP_001316019.1:p.Gly337= |