HGVS | Genome Assembly |
---|---|
NC_000020.11:g.35438197A>T , CM000682.2:g.35438197A>T | GRCh38 |
NC_000020.10:g.34025977A>T , CM000682.1:g.34025977A>T | GRCh37 |
NC_000020.9:g.33489391A>T | NCBI36 |
NG_008076.2:g.5023T>A | |
NG_008076.3:g.21550T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374369.8:c.-269T>A MANE Select | ENSP00000363489.3:n.-269T>A | |
ENST00000374369.7:c.-269T>A | ENSP00000363489.3:n.-269T>A | |
ENST00000374372.1:c.-241-28T>A | ENSP00000363492.1:n.-241-28T>A | |
XM_011529075.1:c.-241-28T>A | XP_011527377.1:n.-241-28T>A | |
XM_011529076.1:c.-241-28T>A | XP_011527378.1:n.-241-28T>A | |
NM_001319138.1:c.-241-28T>A | NP_001306067.1:n.-241-28T>A | |
NM_000557.5:c.-269T>A MANE Select | NP_000548.2:n.-269T>A | |
NM_001319138.2:c.-241-28T>A | NP_001306067.1:n.-241-28T>A |