HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44372318A= , CM000679.2:g.44372318A= | GRCh38 |
NC_000017.10:g.42449686A= , CM000679.1:g.42449686A= | GRCh37 |
NC_000017.9:g.39805212A= | NCBI36 |
NG_008331.1:g.22188T= , LRG_479:g.22188T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262407.6:c.*46T= MANE Select | ENSP00000262407.5:n.*46T= | |
ENST00000648408.1:c.2480T= | ||
ENST00000262407.5:c.*46T= | ENSP00000262407.5:n.*46T= | |
ENST00000587295.5:c.359T= | ||
ENST00000588098.1:c.143T= | ||
NM_000419.3:c.*46T= , LRG_479t1:c.*46T= | NP_000410.2:n.*46T= | |
XM_011524749.1:c.*46T= | XP_011523051.1:n.*46T= | |
XM_011524750.1:c.*46T= | XP_011523052.1:n.*46T= | |
NM_000419.4:c.*46T= | NP_000410.2:n.*46T= | |
NM_000419.5:c.*46T= MANE Select | NP_000410.2:n.*46T= |