HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81357827C>G , CM000678.2:g.81357827C>G | GRCh38 |
NC_000016.9:g.81391432C>G , CM000678.1:g.81391432C>G | GRCh37 |
NC_000016.8:g.79948933C>G | NCBI36 |
NG_009007.1:g.47862C>G , LRG_242:g.47862C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.*577C>G | ENSP00000498114.1:n.*577C>G | |
ENST00000648994.2:c.869C>G MANE Select | ENSP00000497351.1:p.Ala290Gly | |
ENST00000650388.1:c.403C>G | ENSP00000498081.1:n.403C>G | |
ENST00000568107.2:c.869C>G | ENSP00000476795.1:p.Ala290Gly | |
NM_022041.3:c.869C>G , LRG_242t1:c.869C>G | NP_071324.1:p.Ala290Gly | |
XM_017023734.1:c.230C>G | XP_016879223.1:p.Ala77Gly | |
NM_001377486.1:c.230C>G | NP_001364415.1:p.Ala77Gly | |
NM_022041.4:c.869C>G MANE Select | NP_071324.1:p.Ala290Gly |