HGVS | Genome Assembly |
---|---|
NC_000002.12:g.201623464A>T , CM000664.2:g.201623464A>T | GRCh38 |
NC_000002.11:g.202488187A>T , CM000664.1:g.202488187A>T | GRCh37 |
NC_000002.10:g.202196432A>T | NCBI36 |
NG_032049.1:g.25066T>A | |
NG_051007.1:g.719T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000621467.5:c.*791T>A | ENSP00000480508.2:n.*791T>A | |
ENST00000686475.1:n.1958T>A | ||
ENST00000409883.7:c.*791T>A MANE Select | ENSP00000386264.2:n.*791T>A | |
ENST00000409444.6:c.*791T>A | ENSP00000387203.2:n.*791T>A | |
ENST00000409883.6:c.*791T>A | ENSP00000386264.2:n.*791T>A | |
ENST00000495329.1:n.1157T>A | ||
NM_001044385.2:c.*791T>A | NP_001037850.1:n.*791T>A | |
NM_152388.3:c.*791T>A | NP_689601.2:n.*791T>A | |
NM_001044385.3:c.*791T>A MANE Select | NP_001037850.1:n.*791T>A | |
NM_152388.4:c.*791T>A | NP_689601.2:n.*791T>A |