HGVS | Genome Assembly |
---|---|
NC_000016.10:g.20389104G= , CM000678.2:g.20389104G= | GRCh38 |
NC_000016.9:g.20400426G= , CM000678.1:g.20400426G= | GRCh37 |
NC_000016.8:g.20307927G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000302451.9:c.203-4253C= MANE Select | ENSP00000305465.4:n.203-4253C= | |
ENST00000302451.8:c.203-4253C= | ENSP00000305465.4:n.203-4253C= | |
ENST00000575561.1:c.203-195C= | ENSP00000459161.1:n.203-195C= | |
NM_174924.1:c.203-4253C= | NP_777584.1:n.203-4253C= | |
XM_006721024.1:c.203-4253C= | XP_006721087.1:n.203-4253C= | |
XM_011545764.1:c.203-4253C= | XP_011544066.1:n.203-4253C= | |
XM_011545765.1:c.203-4253C= | XP_011544067.1:n.203-4253C= | |
XR_950754.1:n.457-4253C= | ||
NM_174924.2:c.203-4253C= MANE Select | NP_777584.1:n.203-4253C= |