HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86668098C>A , CM000670.2:g.86668098C>A | GRCh38 |
NC_000008.10:g.87680326C>A , CM000670.1:g.87680326C>A | GRCh37 |
NC_000008.9:g.87749442C>A | NCBI36 |
NG_016980.1:g.80578G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320005.6:c.564G>T MANE Select | ENSP00000316605.5:p.Leu188Phe | |
ENST00000681746.1:c.564G>T | ENSP00000505959.1:p.Leu188Phe | |
ENST00000320005.5:c.564G>T | ENSP00000316605.5:p.Leu188Phe | |
NM_019098.4:c.564G>T | NP_061971.3:p.Leu188Phe | |
XM_011517138.1:c.150G>T | XP_011515440.1:p.Leu50Phe | |
XM_011517138.2:c.150G>T | XP_011515440.1:p.Leu50Phe | |
NM_019098.5:c.564G>T MANE Select | NP_061971.3:p.Leu188Phe |