HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67436148T= , CM000678.2:g.67436148T= | GRCh38 |
NC_000016.9:g.67470051T= , CM000678.1:g.67470051T= | GRCh37 |
NC_000016.8:g.66027552T= | NCBI36 |
NG_011482.1:g.50039A= | |
NG_016549.1:g.10016T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326152.6:c.664+6T= MANE Select | ENSP00000316786.5:n.664+6T= | |
ENST00000326152.5:c.664+6T= | ENSP00000316786.5:n.664+6T= | |
ENST00000567684.2:n.527+6T= | ||
NM_000196.3:c.664+6T= | NP_000187.3:n.664+6T= | |
NM_000196.4:c.664+6T= MANE Select | NP_000187.3:n.664+6T= |