HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240873882C= , CM000664.2:g.240873882C= | GRCh38 |
NC_000002.11:g.241813299C= , CM000664.1:g.241813299C= | GRCh37 |
NC_000002.10:g.241461972C= | NCBI36 |
NG_008005.1:g.10138C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.596-96C= MANE Select | ENSP00000302620.3:n.596-96C= | |
ENST00000307503.3:c.596-96C= | ENSP00000302620.3:n.596-96C= | |
ENST00000476698.1:n.332+833C= | ||
NM_000030.2:c.596-96C= | NP_000021.1:n.596-96C= | |
NM_000030.3:c.596-96C= MANE Select | NP_000021.1:n.596-96C= |