HGVS | Genome Assembly |
---|---|
NC_000011.10:g.299496C= , CM000673.2:g.299496C= | GRCh38 |
NC_000011.9:g.299496C= , CM000673.1:g.299496C= | GRCh37 |
NC_000011.8:g.289496C= | NCBI36 |
NG_032892.1:g.5031G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382614.2:c.-6G= MANE Select | ENSP00000372059.2:n.-6G= | |
NM_001025295.2:c.-6G= | NP_001020466.1:n.-6G= | |
NM_001025295.3:c.-6G= MANE Select | NP_001020466.1:n.-6G= |