HGVS | Genome Assembly |
---|---|
NC_000017.11:g.82727477T= , CM000679.2:g.82727477T= | GRCh38 |
NC_000017.10:g.80685353T= , CM000679.1:g.80685353T= | GRCh37 |
NC_000017.9:g.78278642T= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000269373.11:c.*306T= MANE Select | ENSP00000269373.6:n.*306T= | |
ENST00000269373.10:c.*306T= | ENSP00000269373.6:n.*306T= | |
ENST00000571594.1:c.53+310T= | ENSP00000459751.1:n.53+310T= | |
ENST00000574832.5:c.*1193T= | ENSP00000460869.1:n.*1193T= | |
NM_024619.3:c.*306T= | NP_078895.2:n.*306T= | |
NR_046408.1:n.1414T= | ||
XM_024450948.1:c.*306T= | XP_024306716.1:n.*306T= | |
NM_024619.4:c.*306T= MANE Select | NP_078895.2:n.*306T= | |
NR_046408.2:n.1414T= |