Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197009485T= , CM000663.2:g.197009485T= | GRCh38 |
| NC_000001.10:g.196978615T= , CM000663.1:g.196978615T= | GRCh37 |
| NC_000001.9:g.195245238T= | NCBI36 |
| NG_016365.1:g.36949T= , LRG_227:g.36949T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256785.5:c.*802T= MANE Select | ENSP00000256785.4:n.*802T= | |
| ENST00000256785.4:c.*802T= | ENSP00000256785.4:n.*802T= | |
| NM_030787.3:c.*802T= , LRG_227t1:c.*802T= | NP_110414.1:n.*802T= | |
| XM_011510020.1:c.*802T= | XP_011508322.1:n.*802T= | |
| XM_011510020.2:c.*802T= | XP_011508322.1:n.*802T= | |
| NM_030787.4:c.*802T= MANE Select | NP_110414.1:n.*802T= |