HGVS | Genome Assembly |
---|---|
NC_000017.11:g.50185491A= , CM000679.2:g.50185491A= | GRCh38 |
NC_000017.10:g.48262852A= , CM000679.1:g.48262852A= | GRCh37 |
NC_000017.9:g.45617851A= | NCBI36 |
NG_007400.1:g.21149T= , LRG_1:g.21149T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225964.10:c.*11T= MANE Select | ENSP00000225964.6:n.*11T= | |
ENST00000225964.9:c.*11T= | ENSP00000225964.5:n.*11T= | |
NM_000088.3:c.*11T= , LRG_1t1:c.*11T= | NP_000079.2:n.*11T= | |
XM_005257058.3:c.*11T= | XP_005257115.2:n.*11T= | |
XM_005257059.3:c.*11T= | XP_005257116.2:n.*11T= | |
XM_011524341.1:c.*11T= | XP_011522643.1:n.*11T= | |
XM_005257058.4:c.*11T= | XP_005257115.2:n.*11T= | |
XM_005257059.4:c.*11T= | XP_005257116.2:n.*11T= | |
NM_000088.4:c.*11T= MANE Select | NP_000079.2:n.*11T= |