Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.40099262A>G , CM000679.2:g.40099262A>G | GRCh38 |
| NC_000017.10:g.38255515A>G , CM000679.1:g.38255515A>G | GRCh37 |
| NC_000017.9:g.35509041A>G | NCBI36 |
| NG_033084.1:g.6464T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000246672.4:c.31+802T>C MANE Select | ENSP00000246672.3:n.31+802T>C | |
| ENST00000246672.3:c.31+802T>C | ENSP00000246672.3:n.31+802T>C | |
| NM_021724.4:c.31+802T>C | NP_068370.1:n.31+802T>C | |
| NM_021724.5:c.31+802T>C MANE Select | NP_068370.1:n.31+802T>C |