HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189003234T= , CM000664.2:g.189003234T= | GRCh38 |
NC_000002.11:g.189867960T= , CM000664.1:g.189867960T= | GRCh37 |
NC_000002.10:g.189576205T= | NCBI36 |
NG_007404.1:g.33862T= , LRG_3:g.33862T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.2454+172T= | ENSP00000415346.2:n.2454+172T= | |
ENST00000304636.9:c.2553+172T= MANE Select | ENSP00000304408.4:n.2553+172T= | |
ENST00000304636.7:c.2553+172T= | ENSP00000304408.3:n.2553+172T= | |
ENST00000317840.9:c.2527+198T= | ENSP00000315243.6:n.2527+198T= | |
NM_000090.3:c.2553+172T= , LRG_3t1:c.2553+172T= | NP_000081.1:n.2553+172T= | |
NM_000090.4:c.2553+172T= MANE Select | NP_000081.2:n.2553+172T= |