HGVS | Genome Assembly |
---|---|
NC_000023.11:g.53378318T>A , CM000685.2:g.53378318T>A | GRCh38 |
NC_000023.10:g.53405239T>A , CM000685.1:g.53405239T>A | GRCh37 |
NC_000023.9:g.53421964T>A | NCBI36 |
NG_006988.2:g.49353A>T , LRG_773:g.49353A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000322213.9:c.*1785A>T MANE Select | ENSP00000323421.3:n.*1785A>T | |
ENST00000675504.1:c.*1785A>T | ENSP00000502524.1:n.*1785A>T | |
ENST00000322213.8:c.*1785A>T | ENSP00000323421.3:n.*1785A>T | |
ENST00000375340.10:c.*1785A>T | ENSP00000364489.7:n.*1785A>T | |
NM_001281463.1:c.*1785A>T , LRG_773t1:c.*1785A>T | NP_001268392.1:n.*1785A>T | |
NM_006306.3:c.*1785A>T , LRG_773t2:c.*1785A>T | NP_006297.2:n.*1785A>T | |
NM_006306.4:c.*1785A>T MANE Select | NP_006297.2:n.*1785A>T |