HGVS | Genome Assembly |
---|---|
NC_000023.11:g.74529365A>T , CM000685.2:g.74529365A>T | GRCh38 |
NC_000023.10:g.73749200A>T , CM000685.1:g.73749200A>T | GRCh37 |
NC_000023.9:g.73665925A>T | NCBI36 |
NG_011641.1:g.113116A>T | |
NG_011641.2:g.113116A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000587091.6:c.1323A>T MANE Select | ENSP00000465734.1:p.Pro441= | |
ENST00000636771.1:c.1232A>T | ||
ENST00000587091.5:c.1323A>T | ENSP00000465734.1:p.Pro441= | |
ENST00000590447.1:c.611-1968A>T | ||
NM_006517.4:c.1323A>T | NP_006508.2:p.Pro441= | |
XM_005262294.1:c.1171-1968A>T | XP_005262351.1:n.1171-1968A>T | |
NM_006517.5:c.1323A>T MANE Select | NP_006508.2:p.Pro441= |