HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33005731C>A , CM000668.2:g.33005731C>A | GRCh38 |
NC_000006.11:g.32973508C>A , CM000668.1:g.32973508C>A | GRCh37 |
NC_000006.10:g.33081486C>A | NCBI36 |
NG_012007.1:g.8882G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000229829.7:c.*1107G>T MANE Select | ENSP00000229829.3:n.*1107G>T | |
ENST00000229829.6:c.*1107G>T | ENSP00000229829.3:n.*1107G>T | |
NM_002119.3:c.*1107G>T | NP_002110.1:n.*1107G>T | |
NM_002119.4:c.*1107G>T MANE Select | NP_002110.1:n.*1107G>T |