HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69353362T>C , CM000674.2:g.69353362T>C | GRCh38 |
NC_000012.11:g.69747142T>C , CM000674.1:g.69747142T>C | GRCh37 |
NC_000012.10:g.68033409T>C | NCBI36 |
NG_008195.1:g.10009T>C , LRG_768:g.10009T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.*143T>C MANE Select | ENSP00000261267.2:n.*143T>C | |
ENST00000261267.6:c.*143T>C | ENSP00000261267.2:n.*143T>C | |
ENST00000549690.1:c.*97T>C | ENSP00000449898.1:n.*97T>C | |
NM_000239.2:c.*143T>C , LRG_768t1:c.*143T>C | NP_000230.1:n.*143T>C | |
NM_000239.3:c.*143T>C MANE Select | NP_000230.1:n.*143T>C |