HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94423065G= , CM000669.2:g.94423065G= | GRCh38 |
NC_000007.13:g.94052377G= , CM000669.1:g.94052377G= | GRCh37 |
NC_000007.12:g.93890313G= | NCBI36 |
NG_007405.1:g.33505G= , LRG_2:g.33505G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.2512G= MANE Select | ENSP00000297268.6:p.Gly838= | |
ENST00000297268.10:c.2512G= | ENSP00000297268.6:p.Gly838= | |
ENST00000481570.5:n.595G= | ||
ENST00000497316.5:n.909G= | ||
ENST00000620463.1:c.2506G= | ENSP00000477719.1:p.Gly836= | |
NM_000089.3:c.2512G= , LRG_2t1:c.2512G= | NP_000080.2:p.Gly838= | |
NM_000089.4:c.2512G= MANE Select | NP_000080.2:p.Gly838= |