HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86575511A>G , CM000670.2:g.86575511A>G | GRCh38 |
NC_000008.10:g.87587739A>G , CM000670.1:g.87587739A>G | GRCh37 |
NC_000008.9:g.87656855A>G | NCBI36 |
NG_016980.1:g.173165T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.*293T>C MANE Select | ENSP00000316605.5:n.*293T>C | |
ENST00000681546.1:n.2543T>C | ||
ENST00000681746.1:c.*1134T>C | ENSP00000505959.1:n.*1134T>C | |
ENST00000320005.5:c.*293T>C | ENSP00000316605.5:n.*293T>C | |
ENST00000517327.5:c.276+3178T>C | ENSP00000428329.1:n.276+3178T>C | |
NM_019098.4:c.*293T>C | NP_061971.3:n.*293T>C | |
XM_011517138.1:c.*293T>C | XP_011515440.1:n.*293T>C | |
XM_011517138.2:c.*293T>C | XP_011515440.1:n.*293T>C | |
NM_019098.5:c.*293T>C MANE Select | NP_061971.3:n.*293T>C |