HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071966G>A , CM000667.2:g.111071966G>A | GRCh38 |
NC_000005.9:g.110407664G>A , CM000667.1:g.110407664G>A | GRCh37 |
NC_000005.8:g.110435563G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.76G>A MANE Select | ENSP00000339804.3:p.Val26Met | |
ENST00000344895.3:c.76G>A | ENSP00000339804.3:p.Val26Met | |
ENST00000420978.6:c.76G>A | ENSP00000399099.2:p.Val26Met | |
NM_033035.4:c.76G>A | NP_149024.1:p.Val26Met | |
NR_045089.1:n.1480G>A | ||
NM_033035.5:c.76G>A MANE Select | NP_149024.1:p.Val26Met | |
NR_045089.2:n.1498G>A |