HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32104930T= , CM000684.2:g.32104930T= | GRCh38 |
NC_000022.10:g.32500917T= , CM000684.1:g.32500917T= | GRCh37 |
NC_000022.9:g.30830917T= | NCBI36 |
NG_017045.1:g.66899T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266088.9:c.1771+39T= MANE Select | ENSP00000266088.4:n.1771+39T= | |
ENST00000266088.8:c.1771+39T= | ENSP00000266088.4:n.1771+39T= | |
ENST00000543737.2:c.1390+39T= | ENSP00000444898.1:n.1390+39T= | |
NM_000343.3:c.1771+39T= | NP_000334.1:n.1771+39T= | |
NM_001256314.1:c.1390+39T= | NP_001243243.1:n.1390+39T= | |
XR_938173.1:n.591+1908A= | ||
XR_938174.1:n.486+14925A= | ||
NM_000343.4:c.1771+39T= MANE Select | NP_000334.1:n.1771+39T= | |
NM_001256314.2:c.1390+39T= | NP_001243243.1:n.1390+39T= |