HGVS | Genome Assembly |
---|---|
NC_000014.9:g.22843405C>G , CM000676.2:g.22843405C>G | GRCh38 |
NC_000014.8:g.23312614C>G , CM000676.1:g.23312614C>G | GRCh37 |
NC_000014.7:g.22382454C>G | NCBI36 |
NG_046989.1:g.11873C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311852.11:c.837C>G MANE Select | ENSP00000308208.6:p.Ile279Met | |
ENST00000548162.2:c.837C>G | ENSP00000506068.1:p.Ile279Met | |
ENST00000680097.1:c.*152C>G | ENSP00000506631.1:n.*152C>G | |
ENST00000680941.1:c.*235C>G | ENSP00000506378.1:n.*235C>G | |
ENST00000311852.10:c.837C>G | ENSP00000308208.6:p.Ile279Met | |
ENST00000548162.1:n.1079C>G | ||
NM_004995.3:c.837C>G | NP_004986.1:p.Ile279Met | |
NM_004995.4:c.837C>G MANE Select | NP_004986.1:p.Ile279Met |