HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21196890G= , CM000674.2:g.21196890G= | GRCh38 |
NC_000012.11:g.21349824G= , CM000674.1:g.21349824G= | GRCh37 |
NC_000012.10:g.21241091G= | NCBI36 |
NG_011745.1:g.70697G= , LRG_1022:g.70697G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.728-56G= MANE Select | ENSP00000256958.2:n.728-56G= | |
ENST00000256958.2:c.728-56G= | ENSP00000256958.2:n.728-56G= | |
NM_006446.4:c.728-56G= , LRG_1022t1:c.728-56G= | NP_006437.3:n.728-56G= | |
NM_006446.5:c.728-56G= MANE Select | NP_006437.3:n.728-56G= |