HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67740420C= , CM000666.2:g.67740420C= | GRCh38 |
NC_000004.11:g.68606138C= , CM000666.1:g.68606138C= | GRCh37 |
NC_000004.10:g.68288733C= | NCBI36 |
NG_009293.1:g.20667G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.*60G= MANE Select | ENSP00000226413.5:n.*60G= | |
ENST00000226413.4:c.*60G= | ENSP00000226413.4:n.*60G= | |
NM_000406.2:c.*60G= | NP_000397.1:n.*60G= | |
NM_001012763.1:c.*169G= | NP_001012781.1:n.*169G= | |
NM_000406.3:c.*60G= MANE Select | NP_000397.1:n.*60G= | |
NM_001012763.2:c.*169G= | NP_001012781.1:n.*169G= |