HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33004640G= , CM000668.2:g.33004640G= | GRCh38 |
NC_000006.11:g.32972417G= , CM000668.1:g.32972417G= | GRCh37 |
NC_000006.10:g.33080395G= | NCBI36 |
NG_012007.1:g.9973C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000229829.7:c.*2198C= MANE Select | ENSP00000229829.3:n.*2198C= | |
ENST00000229829.6:c.*2198C= | ENSP00000229829.3:n.*2198C= | |
NM_002119.3:c.*2198C= | NP_002110.1:n.*2198C= | |
NM_002119.4:c.*2198C= MANE Select | NP_002110.1:n.*2198C= |