HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151769T>G , CM000681.2:g.55151769T>G | GRCh38 |
NC_000019.9:g.55663137T>G , CM000681.1:g.55663137T>G | GRCh37 |
NC_000019.8:g.60354949T>G | NCBI36 |
NG_007866.2:g.10964A>C , LRG_432:g.10964A>C | |
NG_011829.2:g.2470A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.*65A>C MANE Select | ENSP00000341838.5:n.*65A>C | |
ENST00000585806.5:n.697A>C | ||
NM_000363.4:c.*65A>C , LRG_432t1:c.*65A>C | NP_000354.4:n.*65A>C | |
NM_000363.5:c.*65A>C MANE Select | NP_000354.4:n.*65A>C |