HGVS | Genome Assembly |
---|---|
NC_000016.10:g.23211223G= , CM000678.2:g.23211223G= | GRCh38 |
NC_000016.9:g.23222544G= , CM000678.1:g.23222544G= | GRCh37 |
NC_000016.8:g.23130045G= | NCBI36 |
NG_011909.1:g.33505G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000300061.3:c.1177-811G= MANE Select | ENSP00000300061.2:n.1177-811G= | |
ENST00000300061.2:c.1177-811G= | ENSP00000300061.2:n.1177-811G= | |
NM_001039.3:c.1177-811G= | NP_001030.2:n.1177-811G= | |
NM_001039.4:c.1177-811G= MANE Select | NP_001030.2:n.1177-811G= |