HGVS | Genome Assembly |
---|---|
NC_000014.9:g.93218656G= , CM000676.2:g.93218656G= | GRCh38 |
NC_000014.8:g.93685002G= , CM000676.1:g.93685002G= | GRCh37 |
NC_000014.7:g.92754755G= | NCBI36 |
NG_051089.1:g.16601G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000013070.11:c.731G= MANE Select | ENSP00000013070.6:p.Gly244= | |
ENST00000013070.10:c.731G= | ENSP00000013070.6:p.Gly244= | |
ENST00000416753.5:c.503G= | ENSP00000391706.2:p.Gly168= | |
ENST00000553674.1:c.*432G= | ENSP00000450470.1:n.*432G= | |
ENST00000553857.5:c.378+3375G= | ||
ENST00000556871.5:c.440G= | ENSP00000451022.1:p.Gly147= | |
NM_175748.3:c.731G= | NP_786924.2:p.Gly244= | |
NR_038150.1:n.833G= | ||
NM_175748.4:c.731G= MANE Select | NP_786924.2:p.Gly244= | |
NR_038150.2:n.633G= |