HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69353384T= , CM000674.2:g.69353384T= | GRCh38 |
NC_000012.11:g.69747164T= , CM000674.1:g.69747164T= | GRCh37 |
NC_000012.10:g.68033431T= | NCBI36 |
NG_008195.1:g.10031T= , LRG_768:g.10031T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.*165T= MANE Select | ENSP00000261267.2:n.*165T= | |
ENST00000261267.6:c.*165T= | ENSP00000261267.2:n.*165T= | |
ENST00000549690.1:c.*119T= | ENSP00000449898.1:n.*119T= | |
NM_000239.2:c.*165T= , LRG_768t1:c.*165T= | NP_000230.1:n.*165T= | |
NM_000239.3:c.*165T= MANE Select | NP_000230.1:n.*165T= |