Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22623656C>A , CM000673.2:g.22623656C>A | GRCh38 |
| NC_000011.9:g.22645202C>A , CM000673.1:g.22645202C>A | GRCh37 |
| NC_000011.8:g.22601778C>A | NCBI36 |
| NG_007425.1:g.7186G>T , LRG_527:g.7186G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022725.4:c.*1030G>T MANE Select | NP_073562.1:n.*1030G>T |
| ENST00000327470.6:c.*1030G>T MANE Select | ENSP00000330875.3:n.*1030G>T |
| NM_022725.3:c.*1030G>T , LRG_527t1:c.*1030G>T | NP_073562.1:n.*1030G>T |
| ENST00000327470.4:c.*1030G>T | ENSP00000330875.3:n.*1030G>T |