Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303784T= , CM000675.2:g.48303784T= | GRCh38 |
| NC_000013.10:g.48877920T= , CM000675.1:g.48877920T= | GRCh37 |
| NC_000013.9:g.47775921T= | NCBI36 |
| NG_009009.1:g.5038T= , LRG_517:g.5038T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.-129T= MANE Select | ENSP00000267163.4:n.-129T= | |
| ENST00000646097.1:c.-129T= | ENSP00000496556.1:n.-129T= | |
| ENST00000650461.1:c.-129T= | ENSP00000497193.1:n.-129T= | |
| ENST00000267163.4:c.-129T= | ENSP00000267163.4:n.-129T= | |
| ENST00000467505.5:c.-129T= | ENSP00000434702.1:n.-129T= | |
| ENST00000525036.1:n.34T= | ||
| NM_000321.2:c.-129T= , LRG_517t1:c.-129T= | NP_000312.2:n.-129T= | |
| NM_000321.3:c.-129T= MANE Select | NP_000312.2:n.-129T= |