HGVS | Genome Assembly |
---|---|
NC_000005.10:g.53560661A= , CM000667.2:g.53560661A= | GRCh38 |
NC_000005.9:g.52856491A= , CM000667.1:g.52856491A= | GRCh37 |
NC_000005.8:g.52892248A= | NCBI36 |
NG_008200.1:g.5027A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296684.10:c.-2A= MANE Select | ENSP00000296684.5:n.-2A= | |
ENST00000296684.9:c.-2A= | ENSP00000296684.5:n.-2A= | |
ENST00000502423.5:c.-2A= | ENSP00000422177.1:n.-2A= | |
ENST00000506974.5:c.-2A= | ENSP00000425967.1:n.-2A= | |
ENST00000507026.5:c.-2A= | ENSP00000424993.1:n.-2A= | |
NM_002495.2:c.-2A= | NP_002486.1:n.-2A= | |
XM_005248525.3:c.-2A= | XP_005248582.1:n.-2A= | |
XM_011543414.1:c.-2A= | XP_011541716.1:n.-2A= | |
NM_001318051.1:c.-2A= | NP_001304980.1:n.-2A= | |
NM_002495.3:c.-2A= | NP_002486.1:n.-2A= | |
NR_134473.1:n.29A= | ||
NR_134474.1:n.29A= | ||
NR_134475.1:n.29A= | ||
XM_017009491.1:c.-2A= | XP_016864980.1:n.-2A= | |
NM_002495.4:c.-2A= MANE Select | NP_002486.1:n.-2A= | |
NM_001318051.2:c.-2A= | NP_001304980.1:n.-2A= | |
NR_134473.2:n.23A= | ||
NR_134474.2:n.23A= | ||
NR_134475.2:n.23A= |