HGVS | Genome Assembly |
---|---|
NC_000008.11:g.20208445T= , CM000670.2:g.20208445T= | GRCh38 |
NC_000008.10:g.20065956T= , CM000670.1:g.20065956T= | GRCh37 |
NC_000008.9:g.20110236T= | NCBI36 |
NG_047013.1:g.16253T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276390.7:c.193-988T= MANE Select | ENSP00000276390.2:n.193-988T= | |
ENST00000276390.6:c.193-988T= | ENSP00000276390.2:n.193-988T= | |
ENST00000519667.1:c.161-988T= | ||
ENST00000520830.1:c.301-988T= | ||
ENST00000523478.5:c.193-996T= | ENSP00000430154.1:n.193-996T= | |
ENST00000523482.5:n.197-988T= | ||
NM_001693.3:c.193-988T= | NP_001684.2:n.193-988T= | |
XR_002956632.1:n.225-988T= | ||
XR_002956633.1:n.225-988T= | ||
NM_001693.4:c.193-988T= MANE Select | NP_001684.2:n.193-988T= |