HGVS | Genome Assembly |
---|---|
NC_000005.10:g.31532391A= , CM000667.2:g.31532391A= | GRCh38 |
NC_000005.9:g.31532498A= , CM000667.1:g.31532498A= | GRCh37 |
NC_000005.8:g.31568255A= | NCBI36 |
NG_051574.1:g.4785T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325366.14:c.-2A= MANE Select | ENSP00000326879.9:n.-2A= | |
ENST00000325366.13:c.-2A= | ENSP00000326879.9:n.-2A= | |
ENST00000504464.5:c.-2A= | ENSP00000430261.1:n.-2A= | |
ENST00000507818.6:c.-2A= | ENSP00000430860.1:n.-2A= | |
ENST00000510659.5:c.-2A= | ENSP00000423039.1:n.-2A= | |
ENST00000511208.2:c.-2A= | ENSP00000428898.1:n.-2A= | |
ENST00000513967.5:c.-2A= | ENSP00000421667.1:n.-2A= | |
ENST00000515409.5:n.97A= | ||
ENST00000517780.1:n.97A= | ||
NM_018356.2:c.-2A= | NP_060826.2:n.-2A= | |
XM_005248319.2:c.-573A= | XP_005248376.1:n.-573A= | |
XM_006714479.1:c.-162A= | XP_006714542.1:n.-162A= | |
XM_006714480.2:c.-484A= | XP_006714543.1:n.-484A= | |
XM_011514062.1:c.-2A= | XP_011512364.1:n.-2A= | |
NR_134298.1:n.126A= | ||
XM_006714479.2:c.-162A= | XP_006714542.1:n.-162A= | |
XM_006714480.3:c.-484A= | XP_006714543.1:n.-484A= | |
XM_011514062.3:c.-2A= | XP_011512364.1:n.-2A= | |
XM_017009607.1:c.-2A= | XP_016865096.1:n.-2A= | |
XM_017009608.2:c.-2A= | XP_016865097.1:n.-2A= | |
XM_017009609.1:c.-162A= | XP_016865098.1:n.-162A= | |
XM_017009610.1:c.-576A= | XP_016865099.1:n.-576A= | |
XM_017009611.2:c.-573A= | XP_016865100.1:n.-573A= | |
XM_017009612.2:c.-484A= | XP_016865101.1:n.-484A= | |
XM_017009613.2:c.-576A= | XP_016865102.1:n.-576A= | |
XM_017009614.1:c.-669A= | XP_016865103.1:n.-669A= | |
XM_017009615.1:c.-577A= | XP_016865104.1:n.-577A= | |
XM_017009616.1:c.-481A= | XP_016865105.1:n.-481A= | |
NM_018356.3:c.-2A= MANE Select | NP_060826.2:n.-2A= | |
NR_134298.2:n.91A= |