HGVS | Genome Assembly |
---|---|
NC_000001.11:g.216070461A= , CM000663.2:g.216070461A= | GRCh38 |
NC_000001.10:g.216243803A= , CM000663.1:g.216243803A= | GRCh37 |
NC_000001.9:g.214310426A= | NCBI36 |
NG_009497.1:g.357936T= | |
NG_009497.2:g.357988T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.5858-169T= MANE Select | ENSP00000305941.3:n.5858-169T= | |
ENST00000674083.1:c.5858-169T= | ENSP00000501296.1:n.5858-169T= | |
ENST00000307340.7:c.5858-169T= | ENSP00000305941.3:n.5858-169T= | |
NM_206933.2:c.5858-169T= | NP_996816.2:n.5858-169T= | |
NM_206933.3:c.5858-169T= | NP_996816.2:n.5858-169T= | |
NM_206933.4:c.5858-169T= MANE Select | NP_996816.3:n.5858-169T= |