HGVS | Genome Assembly |
---|---|
NC_000016.10:g.20389098T= , CM000678.2:g.20389098T= | GRCh38 |
NC_000016.9:g.20400420T= , CM000678.1:g.20400420T= | GRCh37 |
NC_000016.8:g.20307921T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000302451.9:c.203-4247A= MANE Select | ENSP00000305465.4:n.203-4247A= | |
ENST00000302451.8:c.203-4247A= | ENSP00000305465.4:n.203-4247A= | |
ENST00000575561.1:c.203-189A= | ENSP00000459161.1:n.203-189A= | |
NM_174924.1:c.203-4247A= | NP_777584.1:n.203-4247A= | |
XM_006721024.1:c.203-4247A= | XP_006721087.1:n.203-4247A= | |
XM_011545764.1:c.203-4247A= | XP_011544066.1:n.203-4247A= | |
XM_011545765.1:c.203-4247A= | XP_011544067.1:n.203-4247A= | |
XR_950754.1:n.457-4247A= | ||
NM_174924.2:c.203-4247A= MANE Select | NP_777584.1:n.203-4247A= |