Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48464853T= , CM000675.2:g.48464853T= | GRCh38 |
| NC_000013.10:g.49038989T= , CM000675.1:g.49038989T= | GRCh37 |
| NC_000013.9:g.47936990T= | NCBI36 |
| NG_009009.1:g.166107T= , LRG_517:g.166107T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.2212-145T= MANE Select | ENSP00000267163.4:n.2212-145T= | |
| ENST00000643064.1:c.194+83410T= | ||
| ENST00000650461.1:c.2212-145T= | ENSP00000497193.1:n.2212-145T= | |
| ENST00000267163.4:c.2212-145T= | ENSP00000267163.4:n.2212-145T= | |
| NM_000321.2:c.2212-145T= , LRG_517t1:c.2212-145T= | NP_000312.2:n.2212-145T= | |
| XM_011535171.1:c.1951-145T= | XP_011533473.1:n.1951-145T= | |
| XM_011535171.2:c.1951-145T= | XP_011533473.1:n.1951-145T= | |
| NM_000321.3:c.2212-145T= MANE Select | NP_000312.2:n.2212-145T= |