HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128849316T= , CM000669.2:g.128849316T= | GRCh38 |
NC_000007.13:g.128489370T= , CM000669.1:g.128489370T= | GRCh37 |
NC_000007.12:g.128276606T= | NCBI36 |
NG_011807.1:g.23888T= , LRG_870:g.23888T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.4952-15T= MANE Select | ENSP00000327145.8:n.4952-15T= | |
ENST00000325888.12:c.4952-15T= | ENSP00000327145.8:n.4952-15T= | |
ENST00000346177.6:c.4952-15T= | ENSP00000344002.6:n.4952-15T= | |
NM_001127487.1:c.4952-15T= | NP_001120959.1:n.4952-15T= | |
NM_001458.4:c.4952-15T= , LRG_870t1:c.4952-15T= | NP_001449.3:n.4952-15T= | |
NM_001127487.2:c.4952-15T= | NP_001120959.1:n.4952-15T= | |
NM_001458.5:c.4952-15T= MANE Select | NP_001449.3:n.4952-15T= |