Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48459756G= , CM000675.2:g.48459756G= | GRCh38 |
| NC_000013.10:g.49033892G= , CM000675.1:g.49033892G= | GRCh37 |
| NC_000013.9:g.47931893G= | NCBI36 |
| NG_009009.1:g.161010G= , LRG_517:g.161010G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.2029G= MANE Select | NP_000312.2:p.Glu677= |
| ENST00000267163.6:c.2029G= MANE Select | ENSP00000267163.4:p.Glu677= |
| NM_000321.2:c.2029G= , LRG_517t1:c.2029G= | NP_000312.2:p.Glu677= |
| ENST00000267163.4:c.2029G= | ENSP00000267163.4:p.Glu677= |
| ENST00000643064.1:c.194+78313G= | |
| ENST00000650461.1:c.2029G= | ENSP00000497193.1:p.Glu677= |
| XM_011535171.1:c.1768G= | XP_011533473.1:p.Glu590= |
| XM_011535171.2:c.1768G= | XP_011533473.1:p.Glu590= |