HGVS | Genome Assembly |
---|---|
NC_000007.14:g.129213112T= , CM000669.2:g.129213112T= | GRCh38 |
NC_000007.13:g.128852953T= , CM000669.1:g.128852953T= | GRCh37 |
NC_000007.12:g.128640189T= | NCBI36 |
NG_023340.1:g.29241T= | |
NG_023340.2:g.29241T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000249373.8:c.*661T= MANE Select | ENSP00000249373.3:n.*661T= | |
ENST00000655644.1:c.*2780T= | ENSP00000499377.1:n.*2780T= | |
ENST00000249373.7:c.*661T= | ENSP00000249373.3:n.*661T= | |
NM_005631.4:c.*661T= | NP_005622.1:n.*661T= | |
XM_011516522.1:c.*661T= | XP_011514824.1:n.*661T= | |
XM_024446891.1:c.*661T= | XP_024302659.1:n.*661T= | |
NM_005631.5:c.*661T= MANE Select | NP_005622.1:n.*661T= |