HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86668100A>T , CM000670.2:g.86668100A>T | GRCh38 |
NC_000008.10:g.87680328A>T , CM000670.1:g.87680328A>T | GRCh37 |
NC_000008.9:g.87749444A>T | NCBI36 |
NG_016980.1:g.80576T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320005.6:c.562T>A MANE Select | ENSP00000316605.5:p.Leu188Met | |
ENST00000681746.1:c.562T>A | ENSP00000505959.1:p.Leu188Met | |
ENST00000320005.5:c.562T>A | ENSP00000316605.5:p.Leu188Met | |
NM_019098.4:c.562T>A | NP_061971.3:p.Leu188Met | |
XM_011517138.1:c.148T>A | XP_011515440.1:p.Leu50Met | |
XM_011517138.2:c.148T>A | XP_011515440.1:p.Leu50Met | |
NM_019098.5:c.562T>A MANE Select | NP_061971.3:p.Leu188Met |