HGVS | Genome Assembly |
---|---|
NC_000001.11:g.155290250A>G , CM000663.2:g.155290250A>G | GRCh38 |
NC_000001.10:g.155260041A>G , CM000663.1:g.155260041A>G | GRCh37 |
NC_000001.9:g.153526665A>G | NCBI36 |
NG_011677.1:g.16185T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342741.6:c.*322T>C MANE Select | ENSP00000339933.4:n.*322T>C | |
ENST00000392414.7:c.*322T>C | ENSP00000376214.3:n.*322T>C | |
NM_000298.5:c.*322T>C | NP_000289.1:n.*322T>C | |
NM_181871.3:c.*322T>C | NP_870986.1:n.*322T>C | |
NM_000298.6:c.*322T>C MANE Select | NP_000289.1:n.*322T>C | |
NM_181871.4:c.*322T>C | NP_870986.1:n.*322T>C |