HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189003992G= , CM000664.2:g.189003992G= | GRCh38 |
NC_000002.11:g.189868718G= , CM000664.1:g.189868718G= | GRCh37 |
NC_000002.10:g.189576963G= | NCBI36 |
NG_007404.1:g.34620G= , LRG_3:g.34620G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.2573G= | ENSP00000415346.2:p.Gly858= | |
ENST00000304636.9:c.2672G= MANE Select | ENSP00000304408.4:p.Gly891= | |
ENST00000304636.7:c.2672G= | ENSP00000304408.3:p.Gly891= | |
ENST00000317840.9:c.2527+956G= | ENSP00000315243.6:n.2527+956G= | |
NM_000090.3:c.2672G= , LRG_3t1:c.2672G= | NP_000081.1:p.Gly891= | |
NM_000090.4:c.2672G= MANE Select | NP_000081.2:p.Gly891= |