HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60645431T= , CM000676.2:g.60645431T= | GRCh38 |
NC_000014.8:g.61112149T= , CM000676.1:g.61112149T= | GRCh37 |
NC_000014.7:g.60181902T= | NCBI36 |
NG_008231.1:g.9007A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000645694.3:c.*852A= MANE Select | ENSP00000494686.1:n.*852A= | |
ENST00000247182.6:c.*852A= | ENSP00000247182.5:n.*852A= | |
ENST00000553535.2:n.1395A= | ||
ENST00000554986.2:c.*852A= | ENSP00000452700.2:n.*852A= | |
ENST00000555955.3:n.2344A= | ||
NM_005982.3:c.*852A= | NP_005973.1:n.*852A= | |
XM_017021602.2:c.*1126A= | XP_016877091.1:n.*1126A= | |
NM_005982.4:c.*852A= MANE Select | NP_005973.1:n.*852A= |