HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320453T= , CM000667.2:g.159320453T= | GRCh38 |
NC_000005.9:g.158747461T= , CM000667.1:g.158747461T= | GRCh37 |
NC_000005.8:g.158680039T= | NCBI36 |
NG_009618.1:g.15021A= , LRG_71:g.15021A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.-81A= | ENSP00000512849.1:n.-81A= | |
ENST00000696751.1:c.*45A= | ENSP00000512850.1:n.*45A= | |
ENST00000231228.3:c.550A= MANE Select | ENSP00000231228.2:p.Asn184= | |
ENST00000231228.2:c.550A= | ENSP00000231228.2:p.Asn184= | |
NM_002187.2:c.550A= , LRG_71t1:c.550A= | NP_002178.2:p.Asn184= | |
XR_001742945.1:n.4T= | ||
NM_002187.3:c.550A= MANE Select | NP_002178.2:p.Asn184= |