HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148826805G= , CM000667.2:g.148826805G= | GRCh38 |
NC_000005.9:g.148206368G= , CM000667.1:g.148206368G= | GRCh37 |
NC_000005.8:g.148186561G= | NCBI36 |
NG_016421.1:g.5213G= | |
NG_016421.2:g.5213G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305988.6:c.-27G= MANE Select | ENSP00000305372.4:n.-27G= | |
ENST00000305988.5:c.-27G= | ENSP00000305372.4:n.-27G= | |
NM_000024.5:c.-27G= | NP_000015.1:n.-27G= | |
NM_000024.6:c.-27G= MANE Select | NP_000015.2:n.-27G= |