HGVS | Genome Assembly |
---|---|
NC_000017.11:g.82727274T= , CM000679.2:g.82727274T= | GRCh38 |
NC_000017.10:g.80685150T= , CM000679.1:g.80685150T= | GRCh37 |
NC_000017.9:g.78278439T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269373.11:c.*103T= MANE Select | ENSP00000269373.6:n.*103T= | |
ENST00000269373.10:c.*103T= | ENSP00000269373.6:n.*103T= | |
ENST00000571594.1:c.53+107T= | ENSP00000459751.1:n.53+107T= | |
ENST00000574832.5:c.*990T= | ENSP00000460869.1:n.*990T= | |
NM_024619.3:c.*103T= | NP_078895.2:n.*103T= | |
NR_046408.1:n.1211T= | ||
XM_024450948.1:c.*103T= | XP_024306716.1:n.*103T= | |
NM_024619.4:c.*103T= MANE Select | NP_078895.2:n.*103T= | |
NR_046408.2:n.1211T= |