Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117819986A= , CM000670.2:g.117819986A= | GRCh38 |
| NC_000008.10:g.118832225A= , CM000670.1:g.118832225A= | GRCh37 |
| NC_000008.9:g.118901406A= | NCBI36 |
| NG_007455.2:g.296834T= , LRG_493:g.296834T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.885-192T= | ||
| ENST00000378204.7:c.1418-192T= MANE Select | ENSP00000367446.3:n.1418-192T= | |
| ENST00000378204.6:c.1418-192T= | ENSP00000367446.2:n.1418-192T= | |
| ENST00000437196.1:c.*309-192T= | ENSP00000407299.1:n.*309-192T= | |
| NM_000127.2:c.1418-192T= , LRG_493t1:c.1418-192T= | NP_000118.2:n.1418-192T= | |
| NM_000127.3:c.1418-192T= MANE Select | NP_000118.2:n.1418-192T= |