Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50920955C>T , CM000676.2:g.50920955C>T | GRCh38 |
| NC_000014.8:g.51387673C>T , CM000676.1:g.51387673C>T | GRCh37 |
| NC_000014.7:g.50457423C>T | NCBI36 |
| NG_012796.1:g.28576G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002863.5:c.772+1G>A MANE Select | NP_002854.3:n.772+1G>A |
| ENST00000216392.8:c.772+1G>A MANE Select | ENSP00000216392.7:n.772+1G>A |
| NM_001163940.1:c.670+1G>A | NP_001157412.1:n.670+1G>A |
| NM_001163940.2:c.670+1G>A | NP_001157412.1:n.670+1G>A |
| NM_002863.4:c.772+1G>A | NP_002854.3:n.772+1G>A |
| ENST00000216392.7:c.772+1G>A | ENSP00000216392.7:n.772+1G>A |
| ENST00000532462.5:c.772+1G>A | ENSP00000431657.1:n.772+1G>A |
| ENST00000544180.6:c.670+1G>A | ENSP00000443787.1:n.670+1G>A |
| ENST00000553872.1:n.573+1G>A |