Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55063651G= , CM000663.2:g.55063651G= | GRCh38 |
| NC_000001.10:g.55529324G= , CM000663.1:g.55529324G= | GRCh37 |
| NC_000001.9:g.55301912G= | NCBI36 |
| NG_009061.1:g.29105G= , LRG_275:g.29105G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.*486G= | ENSP00000501161.2:n.*486G= | |
| ENST00000710286.1:c.*67G= | ENSP00000518176.1:n.*67G= | |
| ENST00000673903.1:c.*67G= | ENSP00000501257.1:n.*67G= | |
| ENST00000302118.5:c.*67G= MANE Select | ENSP00000303208.5:n.*67G= | |
| ENST00000490692.1:n.2692G= | ||
| NM_174936.3:c.*67G= , LRG_275t1:c.*67G= | NP_777596.2:n.*67G= | |
| NR_110451.1:n.1753G= | ||
| XM_011541193.1:c.*67G= | XP_011539495.1:n.*67G= | |
| NM_174936.4:c.*67G= MANE Select | NP_777596.2:n.*67G= | |
| NR_110451.2:n.1753G= |