HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86575775C= , CM000670.2:g.86575775C= | GRCh38 |
NC_000008.10:g.87588003C= , CM000670.1:g.87588003C= | GRCh37 |
NC_000008.9:g.87657119C= | NCBI36 |
NG_016980.1:g.172901G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.*29G= MANE Select | ENSP00000316605.5:n.*29G= | |
ENST00000681546.1:n.2279G= | ||
ENST00000681746.1:c.*870G= | ENSP00000505959.1:n.*870G= | |
ENST00000320005.5:c.*29G= | ENSP00000316605.5:n.*29G= | |
ENST00000517327.5:c.276+2914G= | ENSP00000428329.1:n.276+2914G= | |
NM_019098.4:c.*29G= | NP_061971.3:n.*29G= | |
XM_011517138.1:c.*29G= | XP_011515440.1:n.*29G= | |
XM_011517138.2:c.*29G= | XP_011515440.1:n.*29G= | |
NM_019098.5:c.*29G= MANE Select | NP_061971.3:n.*29G= |