HGVS | Genome Assembly |
---|---|
NC_000008.11:g.81478710A= , CM000670.2:g.81478710A= | GRCh38 |
NC_000008.10:g.82390945A= , CM000670.1:g.82390945A= | GRCh37 |
NC_000008.9:g.82553500A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256104.5:c.*155T= MANE Select | ENSP00000256104.4:n.*155T= | |
ENST00000256104.4:c.*155T= | ENSP00000256104.4:n.*155T= | |
ENST00000518669.5:n.489T= | ||
ENST00000522659.1:c.*430T= | ENSP00000428385.1:n.*430T= | |
NM_001442.2:c.*155T= | NP_001433.1:n.*155T= | |
XR_001745980.1:n.514+16736A= | ||
NM_001442.3:c.*155T= MANE Select | NP_001433.1:n.*155T= |