HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99420527T= , CM000666.2:g.99420527T= | GRCh38 |
NC_000004.11:g.100341684T= , CM000666.1:g.100341684T= | GRCh37 |
NC_000004.10:g.100560707T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437033.7:c.825+6A= MANE Select | ENSP00000414254.2:n.825+6A= | |
ENST00000209665.8:c.861+6A= | ENSP00000209665.4:n.861+6A= | |
ENST00000437033.6:c.825+6A= | ENSP00000414254.2:n.825+6A= | |
ENST00000476959.5:c.885+6A= | ENSP00000420269.1:n.885+6A= | |
ENST00000482593.5:c.654+6A= | ENSP00000420613.1:n.654+6A= | |
NM_000673.4:c.861+6A= | NP_000664.2:n.861+6A= | |
NM_001166504.1:c.885+6A= | NP_001159976.1:n.885+6A= | |
NM_000673.7:c.825+6A= MANE Select | NP_000664.3:n.825+6A= | |
NM_001166504.2:c.885+6A= | NP_001159976.1:n.885+6A= |