HGVS | Genome Assembly |
---|---|
NC_000023.11:g.53378225G>A , CM000685.2:g.53378225G>A | GRCh38 |
NC_000023.10:g.53405146G>A , CM000685.1:g.53405146G>A | GRCh37 |
NC_000023.9:g.53421871G>A | NCBI36 |
NG_006988.2:g.49446C>T , LRG_773:g.49446C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000322213.9:c.*1878C>T MANE Select | ENSP00000323421.3:n.*1878C>T | |
ENST00000675504.1:c.*1878C>T | ENSP00000502524.1:n.*1878C>T | |
ENST00000322213.8:c.*1878C>T | ENSP00000323421.3:n.*1878C>T | |
ENST00000375340.10:c.*1878C>T | ENSP00000364489.7:n.*1878C>T | |
NM_001281463.1:c.*1878C>T , LRG_773t1:c.*1878C>T | NP_001268392.1:n.*1878C>T | |
NM_006306.3:c.*1878C>T , LRG_773t2:c.*1878C>T | NP_006297.2:n.*1878C>T | |
NM_006306.4:c.*1878C>T MANE Select | NP_006297.2:n.*1878C>T |