HGVS | Genome Assembly |
---|---|
NC_000002.12:g.47377258A= , CM000664.2:g.47377258A= | GRCh38 |
NC_000002.11:g.47604397A= , CM000664.1:g.47604397A= | GRCh37 |
NC_000002.10:g.47457901A= | NCBI36 |
NG_012352.2:g.37096A= , LRG_215:g.37096A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263735.9:c.555+181A= MANE Select | ENSP00000263735.4:n.555+181A= | |
ENST00000263735.8:c.555+181A= | ENSP00000263735.4:n.555+181A= | |
ENST00000405271.5:c.639+181A= | ENSP00000385476.1:n.639+181A= | |
ENST00000456133.5:c.639+181A= | ENSP00000410675.1:n.639+181A= | |
ENST00000490733.1:n.404+181A= | ||
NM_002354.2:c.555+181A= , LRG_215t1:c.555+181A= | NP_002345.2:n.555+181A= | |
NM_002354.3:c.555+181A= MANE Select | NP_002345.2:n.555+181A= |