HGVS | Genome Assembly |
---|---|
NC_000017.11:g.56594649G= , CM000679.2:g.56594649G= | GRCh38 |
NC_000017.10:g.54672010G= , CM000679.1:g.54672010G= | GRCh37 |
NC_000017.9:g.52027009G= | NCBI36 |
NG_011958.1:g.5951G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000332822.6:c.426G= MANE Select | ENSP00000328181.4:p.Arg142= | |
ENST00000332822.4:c.426G= | ENSP00000328181.4:p.Arg142= | |
NM_005450.4:c.426G= | NP_005441.1:p.Arg142= | |
NM_005450.6:c.426G= MANE Select | NP_005441.1:p.Arg142= |