HGVS | Genome Assembly |
---|---|
NC_000007.14:g.147918574T= , CM000669.2:g.147918574T= | GRCh38 |
NC_000007.13:g.147615666T= , CM000669.1:g.147615666T= | GRCh37 |
NC_000007.12:g.147246599T= | NCBI36 |
NG_007092.2:g.1807214T= | |
NG_007092.3:g.1807574T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000361727.8:c.2255+14853T= MANE Select | ENSP00000354778.3:n.2255+14853T= | |
ENST00000636870.1:n.2117+14853T= | ||
ENST00000637825.1:n.1738+14853T= | ||
ENST00000361727.7:c.2255+14853T= | ENSP00000354778.3:n.2255+14853T= | |
ENST00000455301.2:n.190+14853T= | ||
ENST00000627772.2:n.428+14853T= | ||
NM_014141.5:c.2255+14853T= | NP_054860.1:n.2255+14853T= | |
XM_006715919.1:c.743+14853T= | XP_006715982.1:n.743+14853T= | |
NM_014141.6:c.2255+14853T= MANE Select | NP_054860.1:n.2255+14853T= |