HGVS | Genome Assembly |
---|---|
NC_000008.11:g.47960342T= , CM000670.2:g.47960342T= | GRCh38 |
NC_000008.10:g.48872902T= , CM000670.1:g.48872902T= | GRCh37 |
NC_000008.9:g.49035455T= | NCBI36 |
NG_023435.1:g.4842A= , LRG_162:g.4842A= | |
NG_032967.1:g.5140T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000518221.5:c.-15+22T= | ENSP00000430329.1:n.-15+22T= | |
NM_005914.3:c.-803T= | NP_005905.2:n.-803T= | |
NM_182746.2:c.-687T= | NP_877423.1:n.-687T= | |
XM_005251234.1:c.-1049T= | XP_005251291.1:n.-1049T= |