HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94423085T= , CM000669.2:g.94423085T= | GRCh38 |
NC_000007.13:g.94052397T= , CM000669.1:g.94052397T= | GRCh37 |
NC_000007.12:g.93890333T= | NCBI36 |
NG_007405.1:g.33525T= , LRG_2:g.33525T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.2532T= MANE Select | ENSP00000297268.6:p.Gly844= | |
ENST00000297268.10:c.2532T= | ENSP00000297268.6:p.Gly844= | |
ENST00000481570.5:n.615T= | ||
ENST00000497316.5:n.929T= | ||
ENST00000620463.1:c.2526T= | ENSP00000477719.1:p.Gly842= | |
NM_000089.3:c.2532T= , LRG_2t1:c.2532T= | NP_000080.2:p.Gly844= | |
NM_000089.4:c.2532T= MANE Select | NP_000080.2:p.Gly844= |