HGVS | Genome Assembly |
---|---|
NC_000012.12:g.5044264G= , CM000674.2:g.5044264G= | GRCh38 |
NC_000012.11:g.5153430G= , CM000674.1:g.5153430G= | GRCh37 |
NC_000012.10:g.5023691G= | NCBI36 |
NG_012198.1:g.5346G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252321.5:c.117G= MANE Select | ENSP00000252321.3:p.Thr39= | |
ENST00000252321.4:c.117G= | ENSP00000252321.3:p.Thr39= | |
NM_002234.3:c.117G= | NP_002225.2:p.Thr39= | |
NM_002234.4:c.117G= MANE Select | NP_002225.2:p.Thr39= |