HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67740434T>C , CM000666.2:g.67740434T>C | GRCh38 |
NC_000004.11:g.68606152T>C , CM000666.1:g.68606152T>C | GRCh37 |
NC_000004.10:g.68288747T>C | NCBI36 |
NG_009293.1:g.20653A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.*46A>G MANE Select | ENSP00000226413.5:n.*46A>G | |
ENST00000226413.4:c.*46A>G | ENSP00000226413.4:n.*46A>G | |
NM_000406.2:c.*46A>G | NP_000397.1:n.*46A>G | |
NM_001012763.1:c.*155A>G | NP_001012781.1:n.*155A>G | |
NM_000406.3:c.*46A>G MANE Select | NP_000397.1:n.*46A>G | |
NM_001012763.2:c.*155A>G | NP_001012781.1:n.*155A>G |