Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.40099341G>A , CM000679.2:g.40099341G>A | GRCh38 |
| NC_000017.10:g.38255594G>A , CM000679.1:g.38255594G>A | GRCh37 |
| NC_000017.9:g.35509120G>A | NCBI36 |
| NG_033084.1:g.6385C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_021724.5:c.31+723C>T MANE Select | NP_068370.1:n.31+723C>T |
| ENST00000246672.4:c.31+723C>T MANE Select | ENSP00000246672.3:n.31+723C>T |
| NM_021724.4:c.31+723C>T | NP_068370.1:n.31+723C>T |
| ENST00000246672.3:c.31+723C>T | ENSP00000246672.3:n.31+723C>T |