HGVS | Genome Assembly |
---|---|
NC_000014.9:g.65074857A= , CM000676.2:g.65074857A= | GRCh38 |
NC_000014.8:g.65541575A= , CM000676.1:g.65541575A= | GRCh37 |
NC_000014.7:g.64611328A= | NCBI36 |
NG_029830.1:g.32653T= , LRG_530:g.32653T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651648.1:c.145-4488T= | ENSP00000498863.1:n.145-4488T= | |
ENST00000341653.6:c.171+18851T= | ENSP00000342482.2:n.171+18851T= | |
NM_001271069.1:c.144+18851T= | NP_001257998.1:n.144+18851T= | |
NM_197957.3:c.171+18851T= | NP_932061.1:n.171+18851T= | |
NM_001271069.2:c.144+18851T= | NP_001257998.1:n.144+18851T= | |
NM_197957.4:c.171+18851T= | NP_932061.1:n.171+18851T= |