HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189003913T= , CM000664.2:g.189003913T= | GRCh38 |
NC_000002.11:g.189868639T= , CM000664.1:g.189868639T= | GRCh37 |
NC_000002.10:g.189576884T= | NCBI36 |
NG_007404.1:g.34541T= , LRG_3:g.34541T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.2563-69T= | ENSP00000415346.2:n.2563-69T= | |
ENST00000304636.9:c.2662-69T= MANE Select | ENSP00000304408.4:n.2662-69T= | |
ENST00000304636.7:c.2662-69T= | ENSP00000304408.3:n.2662-69T= | |
ENST00000317840.9:c.2527+877T= | ENSP00000315243.6:n.2527+877T= | |
ENST00000467886.1:n.222T= | ||
NM_000090.3:c.2662-69T= , LRG_3t1:c.2662-69T= | NP_000081.1:n.2662-69T= | |
NM_000090.4:c.2662-69T= MANE Select | NP_000081.2:n.2662-69T= |