HGVS | Genome Assembly |
---|---|
NC_000012.12:g.14506981C= , CM000674.2:g.14506981C= | GRCh38 |
NC_000012.11:g.14659915C= , CM000674.1:g.14659915C= | GRCh37 |
NC_000012.10:g.14551182C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000240617.10:c.1324G= MANE Select | ENSP00000240617.5:p.Gly442= | |
ENST00000240617.9:c.1324G= | ENSP00000240617.5:p.Gly442= | |
NM_024829.5:c.1324G= | NP_079105.4:p.Gly442= | |
NM_024829.6:c.1324G= MANE Select | NP_079105.4:p.Gly442= |