Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48304058G>A , CM000675.2:g.48304058G>A | GRCh38 |
| NC_000013.10:g.48878194G>A , CM000675.1:g.48878194G>A | GRCh37 |
| NC_000013.9:g.47776195G>A | NCBI36 |
| NG_009009.1:g.5312G>A , LRG_517:g.5312G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.137+9G>A MANE Select | ENSP00000267163.4:n.137+9G>A | |
| ENST00000646097.1:c.137+9G>A | ENSP00000496556.1:n.137+9G>A | |
| ENST00000650461.1:c.137+9G>A | ENSP00000497193.1:n.137+9G>A | |
| ENST00000267163.4:c.137+9G>A | ENSP00000267163.4:n.137+9G>A | |
| ENST00000467505.5:c.137+9G>A | ENSP00000434702.1:n.137+9G>A | |
| ENST00000525036.1:n.299+9G>A | ||
| NM_000321.2:c.137+9G>A , LRG_517t1:c.137+9G>A | NP_000312.2:n.137+9G>A | |
| NM_000321.3:c.137+9G>A MANE Select | NP_000312.2:n.137+9G>A |