HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87727535T= , CM000672.2:g.87727535T= | GRCh38 |
NC_000010.10:g.89487292T= , CM000672.1:g.89487292T= | GRCh37 |
NC_000010.9:g.89477272T= | NCBI36 |
NG_012150.1:g.72817T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000456849.2:c.1086+46T= MANE Select | ENSP00000406157.1:n.1086+46T= | |
ENST00000361175.8:c.1071+46T= | ENSP00000354436.4:n.1071+46T= | |
ENST00000456849.1:c.1086+46T= | ENSP00000406157.1:n.1086+46T= | |
NM_001015880.1:c.1086+46T= | NP_001015880.1:n.1086+46T= | |
NM_004670.3:c.1071+46T= | NP_004661.2:n.1071+46T= | |
NM_001015880.2:c.1086+46T= MANE Select | NP_001015880.1:n.1086+46T= | |
NM_004670.4:c.1071+46T= | NP_004661.2:n.1071+46T= |