HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67754343C= , CM000666.2:g.67754343C= | GRCh38 |
NC_000004.11:g.68620061C= , CM000666.1:g.68620061C= | GRCh37 |
NC_000004.10:g.68302656C= | NCBI36 |
NG_009293.1:g.6744G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.-8G= MANE Select | ENSP00000226413.5:n.-8G= | |
ENST00000226413.4:c.-8G= | ENSP00000226413.4:n.-8G= | |
NM_000406.2:c.-8G= | NP_000397.1:n.-8G= | |
NM_001012763.1:c.-8G= | NP_001012781.1:n.-8G= | |
NM_000406.3:c.-8G= MANE Select | NP_000397.1:n.-8G= | |
NM_001012763.2:c.-8G= | NP_001012781.1:n.-8G= |