HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148826813A>G , CM000667.2:g.148826813A>G | GRCh38 |
NC_000005.9:g.148206376A>G , CM000667.1:g.148206376A>G | GRCh37 |
NC_000005.8:g.148186569A>G | NCBI36 |
NG_016421.1:g.5221A>G | |
NG_016421.2:g.5221A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305988.6:c.-19A>G MANE Select | ENSP00000305372.4:n.-19A>G | |
ENST00000305988.5:c.-19A>G | ENSP00000305372.4:n.-19A>G | |
NM_000024.5:c.-19A>G | NP_000015.1:n.-19A>G | |
NM_000024.6:c.-19A>G MANE Select | NP_000015.2:n.-19A>G |