HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128357350C>T , CM000667.2:g.128357350C>T | GRCh38 |
NC_000005.9:g.127693042C>T , CM000667.1:g.127693042C>T | GRCh37 |
NC_000005.8:g.127720941C>T | NCBI36 |
NG_008750.1:g.185694G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262464.9:c.2600G>A MANE Select | ENSP00000262464.4:p.Arg867Lys | |
ENST00000262464.8:c.2600G>A | ENSP00000262464.4:p.Arg867Lys | |
ENST00000508053.5:c.2600G>A | ENSP00000424571.1:p.Arg867Lys | |
ENST00000508989.5:c.2501G>A | ENSP00000425596.1:p.Arg834Lys | |
ENST00000619499.4:c.2597G>A | ENSP00000482132.1:p.Arg866Lys | |
NM_001999.3:c.2600G>A | NP_001990.2:p.Arg867Lys | |
XM_017009228.2:c.2447G>A | XP_016864717.1:p.Arg816Lys | |
NM_001999.4:c.2600G>A MANE Select | NP_001990.2:p.Arg867Lys |