HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69353545G= , CM000674.2:g.69353545G= | GRCh38 |
NC_000012.11:g.69747325G= , CM000674.1:g.69747325G= | GRCh37 |
NC_000012.10:g.68033592G= | NCBI36 |
NG_008195.1:g.10192G= , LRG_768:g.10192G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.*326G= MANE Select | ENSP00000261267.2:n.*326G= | |
ENST00000261267.6:c.*326G= | ENSP00000261267.2:n.*326G= | |
NM_000239.2:c.*326G= , LRG_768t1:c.*326G= | NP_000230.1:n.*326G= | |
NM_000239.3:c.*326G= MANE Select | NP_000230.1:n.*326G= |