HGVS | Genome Assembly |
---|---|
NC_000014.9:g.93218655G= , CM000676.2:g.93218655G= | GRCh38 |
NC_000014.8:g.93685001G= , CM000676.1:g.93685001G= | GRCh37 |
NC_000014.7:g.92754754G= | NCBI36 |
NG_051089.1:g.16600G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000013070.11:c.730G= MANE Select | ENSP00000013070.6:p.Gly244= | |
ENST00000013070.10:c.730G= | ENSP00000013070.6:p.Gly244= | |
ENST00000416753.5:c.502G= | ENSP00000391706.2:p.Gly168= | |
ENST00000553674.1:c.*431G= | ENSP00000450470.1:n.*431G= | |
ENST00000553857.5:c.378+3374G= | ||
ENST00000556871.5:c.439G= | ENSP00000451022.1:p.Gly147= | |
NM_175748.3:c.730G= | NP_786924.2:p.Gly244= | |
NR_038150.1:n.832G= | ||
NM_175748.4:c.730G= MANE Select | NP_786924.2:p.Gly244= | |
NR_038150.2:n.632G= |