HGVS | Genome Assembly |
---|---|
NC_000014.9:g.93218713C>A , CM000676.2:g.93218713C>A | GRCh38 |
NC_000014.8:g.93685059C>A , CM000676.1:g.93685059C>A | GRCh37 |
NC_000014.7:g.92754812C>A | NCBI36 |
NG_051089.1:g.16658C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000013070.11:c.788C>A MANE Select | ENSP00000013070.6:p.Ser263Tyr | |
ENST00000013070.10:c.788C>A | ENSP00000013070.6:p.Ser263Tyr | |
ENST00000416753.5:c.560C>A | ENSP00000391706.2:p.Ser187Tyr | |
ENST00000553674.1:c.*489C>A | ENSP00000450470.1:n.*489C>A | |
ENST00000553857.5:c.378+3432C>A | ||
ENST00000555329.1:c.33C>A | ||
NM_175748.3:c.788C>A | NP_786924.2:p.Ser263Tyr | |
NR_038150.1:n.890C>A | ||
NM_175748.4:c.788C>A MANE Select | NP_786924.2:p.Ser263Tyr | |
NR_038150.2:n.690C>A |