HGVS | Genome Assembly |
---|---|
NC_000016.10:g.5535851A>G , CM000678.2:g.5535851A>G | GRCh38 |
NC_000016.9:g.5585852A>G , CM000678.1:g.5585852A>G | GRCh37 |
NC_000016.8:g.5525853A>G | NCBI36 |
NG_011881.2:g.301100A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000569895.3:n.344-63051A>G | ||
ENST00000585867.2:n.331-63051A>G | ||
ENST00000641259.1:c.259-63051A>G | ENSP00000493041.1:n.259-63051A>G | |
XM_011522544.1:c.259-63051A>G | XP_011520846.1:n.259-63051A>G | |
XM_017023318.2:c.379-63051A>G | XP_016878807.1:n.379-63051A>G | |
XM_017023319.2:c.379-63051A>G | XP_016878808.1:n.379-63051A>G | |
XM_024450303.1:c.340-63051A>G | XP_024306071.1:n.340-63051A>G |