Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48304081G= , CM000675.2:g.48304081G= | GRCh38 |
| NC_000013.10:g.48878217G= , CM000675.1:g.48878217G= | GRCh37 |
| NC_000013.9:g.47776218G= | NCBI36 |
| NG_009009.1:g.5335G= , LRG_517:g.5335G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.137+32G= MANE Select | ENSP00000267163.4:n.137+32G= | |
| ENST00000646097.1:c.137+32G= | ENSP00000496556.1:n.137+32G= | |
| ENST00000650461.1:c.137+32G= | ENSP00000497193.1:n.137+32G= | |
| ENST00000267163.4:c.137+32G= | ENSP00000267163.4:n.137+32G= | |
| ENST00000467505.5:c.137+32G= | ENSP00000434702.1:n.137+32G= | |
| ENST00000525036.1:n.299+32G= | ||
| NM_000321.2:c.137+32G= , LRG_517t1:c.137+32G= | NP_000312.2:n.137+32G= | |
| NM_000321.3:c.137+32G= MANE Select | NP_000312.2:n.137+32G= |