HGVS | Genome Assembly |
---|---|
NC_000003.12:g.122285198A= , CM000665.2:g.122285198A= | GRCh38 |
NC_000003.11:g.122004045A= , CM000665.1:g.122004045A= | GRCh37 |
NC_000003.10:g.123486735A= | NCBI36 |
NG_009058.1:g.106516A= | |
NG_009058.2:g.106531A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490131.7:c.*7A= | ENSP00000418685.2:n.*7A= | |
ENST00000498619.4:c.*7A= | ENSP00000420194.1:n.*7A= | |
ENST00000638421.1:c.*7A= | ENSP00000492190.1:n.*7A= | |
ENST00000639785.2:c.*7A= MANE Select | ENSP00000491584.2:n.*7A= | |
ENST00000490131.5:c.*7A= | ENSP00000418685.1:n.*7A= | |
ENST00000498619.2:c.*7A= | ENSP00000420194.1:n.*7A= | |
NM_000388.3:c.*7A= | NP_000379.2:n.*7A= | |
NM_001178065.1:c.*7A= | NP_001171536.1:n.*7A= | |
XM_005247836.2:c.*7A= | XP_005247893.1:n.*7A= | |
XM_005247837.2:c.*7A= | XP_005247894.1:n.*7A= | |
XM_006713789.2:c.*7A= | XP_006713852.1:n.*7A= | |
XM_011513237.1:c.*7A= | XP_011511539.1:n.*7A= | |
XM_011513238.1:c.*7A= | XP_011511540.1:n.*7A= | |
XM_011513239.1:c.*7A= | XP_011511541.1:n.*7A= | |
XM_006713789.3:c.*7A= | XP_006713852.1:n.*7A= | |
XM_017007324.1:c.*7A= | XP_016862813.1:n.*7A= | |
XM_017007325.1:c.*7A= | XP_016862814.1:n.*7A= | |
NM_000388.4:c.*7A= MANE Select | NP_000379.3:n.*7A= | |
NM_001178065.2:c.*7A= | NP_001171536.2:n.*7A= |