HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94423073T= , CM000669.2:g.94423073T= | GRCh38 |
NC_000007.13:g.94052385T= , CM000669.1:g.94052385T= | GRCh37 |
NC_000007.12:g.93890321T= | NCBI36 |
NG_007405.1:g.33513T= , LRG_2:g.33513T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.2520T= MANE Select | ENSP00000297268.6:p.Pro840= | |
ENST00000297268.10:c.2520T= | ENSP00000297268.6:p.Pro840= | |
ENST00000481570.5:n.603T= | ||
ENST00000497316.5:n.917T= | ||
ENST00000620463.1:c.2514T= | ENSP00000477719.1:p.Pro838= | |
NM_000089.3:c.2520T= , LRG_2t1:c.2520T= | NP_000080.2:p.Pro840= | |
NM_000089.4:c.2520T= MANE Select | NP_000080.2:p.Pro840= |