HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86574209G>A , CM000670.2:g.86574209G>A | GRCh38 |
NC_000008.10:g.87586437G>A , CM000670.1:g.87586437G>A | GRCh37 |
NC_000008.9:g.87655553G>A | NCBI36 |
NG_016980.1:g.174467C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.*1595C>T MANE Select | ENSP00000316605.5:n.*1595C>T | |
ENST00000681546.1:n.3845C>T | ||
ENST00000681746.1:c.*2436C>T | ENSP00000505959.1:n.*2436C>T | |
ENST00000320005.5:c.*1595C>T | ENSP00000316605.5:n.*1595C>T | |
ENST00000517327.5:c.276+4480C>T | ENSP00000428329.1:n.276+4480C>T | |
NM_019098.4:c.*1595C>T | NP_061971.3:n.*1595C>T | |
XM_011517138.1:c.*1595C>T | XP_011515440.1:n.*1595C>T | |
XM_011517138.2:c.*1595C>T | XP_011515440.1:n.*1595C>T | |
NM_019098.5:c.*1595C>T MANE Select | NP_061971.3:n.*1595C>T |