HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94426014T= , CM000669.2:g.94426014T= | GRCh38 |
NC_000007.13:g.94055326T= , CM000669.1:g.94055326T= | GRCh37 |
NC_000007.12:g.93893262T= | NCBI36 |
NG_007405.1:g.36454T= , LRG_2:g.36454T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.2960T= MANE Select | ENSP00000297268.6:p.Val987= | |
ENST00000297268.10:c.2960T= | ENSP00000297268.6:p.Val987= | |
ENST00000478215.1:n.519T= | ||
ENST00000481570.5:n.2933T= | ||
ENST00000620463.1:c.2954T= | ENSP00000477719.1:p.Val985= | |
NM_000089.3:c.2960T= , LRG_2t1:c.2960T= | NP_000080.2:p.Val987= | |
NM_000089.4:c.2960T= MANE Select | NP_000080.2:p.Val987= |