HGVS | Genome Assembly |
---|---|
NC_000015.10:g.71811648G= , CM000677.2:g.71811648G= | GRCh38 |
NC_000015.9:g.72103988G= , CM000677.1:g.72103988G= | GRCh37 |
NC_000015.8:g.69891042G= | NCBI36 |
NG_009113.2:g.6094G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000617575.5:c.245+39G= MANE Select | ENSP00000482504.1:n.245+39G= | |
ENST00000617575.4:c.245+39G= | ENSP00000482504.1:n.245+39G= | |
ENST00000621098.1:c.245+39G= | ENSP00000479962.1:n.245+39G= | |
ENST00000621736.4:c.-20+39G= | ENSP00000479254.1:n.-20+39G= | |
NM_014249.3:c.245+39G= | NP_055064.1:n.245+39G= | |
NM_016346.3:c.245+39G= | NP_057430.1:n.245+39G= | |
XM_011521146.1:c.-20+39G= | XP_011519448.1:n.-20+39G= | |
NM_014249.4:c.245+39G= MANE Select | NP_055064.1:n.245+39G= | |
NM_016346.4:c.245+39G= | NP_057430.1:n.245+39G= |