HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122508686A>G , CM000672.2:g.122508686A>G | GRCh38 |
NC_000010.10:g.124268202A>G , CM000672.1:g.124268202A>G | GRCh37 |
NC_000010.9:g.124258192A>G | NCBI36 |
NG_011554.1:g.52162A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.1036A>G MANE Select | ENSP00000357980.3:p.Lys346Glu | |
ENST00000648167.1:c.718A>G | ENSP00000498033.1:p.Lys240Glu | |
ENST00000368984.7:c.1036A>G | ENSP00000357980.3:p.Lys346Glu | |
ENST00000420892.1:c.259A>G | ENSP00000412676.1:p.Lys87Glu | |
NM_002775.4:c.1036A>G | NP_002766.1:p.Lys346Glu | |
NM_002775.5:c.1036A>G MANE Select | NP_002766.1:p.Lys346Glu |