HGVS | Genome Assembly |
---|---|
NC_000008.11:g.81478714A= , CM000670.2:g.81478714A= | GRCh38 |
NC_000008.10:g.82390949A= , CM000670.1:g.82390949A= | GRCh37 |
NC_000008.9:g.82553504A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256104.5:c.*151T= MANE Select | ENSP00000256104.4:n.*151T= | |
ENST00000256104.4:c.*151T= | ENSP00000256104.4:n.*151T= | |
ENST00000518669.5:n.485T= | ||
ENST00000521734.1:n.759T= | ||
ENST00000522659.1:c.*426T= | ENSP00000428385.1:n.*426T= | |
NM_001442.2:c.*151T= | NP_001433.1:n.*151T= | |
XR_001745980.1:n.514+16740A= | ||
NM_001442.3:c.*151T= MANE Select | NP_001433.1:n.*151T= |