Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17053943C>T , CM000663.2:g.17053943C>T | GRCh38 |
| NC_000001.10:g.17380438C>T , CM000663.1:g.17380438C>T | GRCh37 |
| NC_000001.9:g.17253025C>T | NCBI36 |
| NG_012340.1:g.5228G>A , LRG_316:g.5228G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375499.8:c.72+5G>A MANE Select | ENSP00000364649.3:n.72+5G>A | |
| ENST00000375499.7:c.72+5G>A | ENSP00000364649.3:n.72+5G>A | |
| ENST00000466613.2:n.84+5G>A | ||
| ENST00000485515.5:n.60+5G>A | ||
| NM_003000.2:c.72+5G>A , LRG_316t1:c.72+5G>A | NP_002991.2:n.72+5G>A | |
| NM_003000.3:c.72+5G>A MANE Select | NP_002991.2:n.72+5G>A |