HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32444633T>C , CM000668.2:g.32444633T>C | GRCh38 |
NC_000006.11:g.32412410T>C , CM000668.1:g.32412410T>C | GRCh37 |
NC_000006.10:g.32520388T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.*12-19T>C MANE Select | ENSP00000378786.2:n.*12-19T>C | |
ENST00000374982.5:c.*12-19T>C | ENSP00000364121.5:n.*12-19T>C | |
ENST00000395388.6:c.*12-19T>C | ENSP00000378786.2:n.*12-19T>C | |
NM_019111.4:c.*12-19T>C | NP_061984.2:n.*12-19T>C | |
NM_019111.5:c.*12-19T>C MANE Select | NP_061984.2:n.*12-19T>C |