HGVS | Genome Assembly |
---|---|
NC_000014.9:g.93218575G= , CM000676.2:g.93218575G= | GRCh38 |
NC_000014.8:g.93684921G= , CM000676.1:g.93684921G= | GRCh37 |
NC_000014.7:g.92754674G= | NCBI36 |
NG_051089.1:g.16520G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000013070.11:c.650G= MANE Select | ENSP00000013070.6:p.Gly217= | |
ENST00000013070.10:c.650G= | ENSP00000013070.6:p.Gly217= | |
ENST00000416753.5:c.422G= | ENSP00000391706.2:p.Gly141= | |
ENST00000553674.1:c.*351G= | ENSP00000450470.1:n.*351G= | |
ENST00000553857.5:c.378+3294G= | ||
ENST00000556871.5:c.359G= | ENSP00000451022.1:p.Gly120= | |
ENST00000557048.1:n.559G= | ||
NM_175748.3:c.650G= | NP_786924.2:p.Gly217= | |
NR_038150.1:n.752G= | ||
NM_175748.4:c.650G= MANE Select | NP_786924.2:p.Gly217= | |
NR_038150.2:n.552G= |