Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48452981T= , CM000675.2:g.48452981T= | GRCh38 |
| NC_000013.10:g.49027117T= , CM000675.1:g.49027117T= | GRCh37 |
| NC_000013.9:g.47925118T= | NCBI36 |
| NG_009009.1:g.154235T= , LRG_517:g.154235T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.1696-12T= MANE Select | NP_000312.2:n.1696-12T= |
| ENST00000267163.6:c.1696-12T= MANE Select | ENSP00000267163.4:n.1696-12T= |
| NM_000321.2:c.1696-12T= , LRG_517t1:c.1696-12T= | NP_000312.2:n.1696-12T= |
| ENST00000267163.4:c.1696-12T= | ENSP00000267163.4:n.1696-12T= |
| ENST00000480491.1:n.395-12T= | |
| ENST00000643064.1:c.194+71538T= | |
| ENST00000650461.1:c.1696-12T= | ENSP00000497193.1:n.1696-12T= |
| XM_011535171.1:c.1435-12T= | XP_011533473.1:n.1435-12T= |
| XM_011535171.2:c.1435-12T= | XP_011533473.1:n.1435-12T= |