HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149980471T>C , CM000667.2:g.149980471T>C | GRCh38 |
NC_000005.9:g.149360034T>C , CM000667.1:g.149360034T>C | GRCh37 |
NC_000005.8:g.149340227T>C | NCBI36 |
NG_007147.2:g.21589T>C , LRG_684:g.21589T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.878T>C MANE Select | ENSP00000286298.4:p.Val293Ala | |
ENST00000286298.4:c.878T>C | ENSP00000286298.4:p.Val293Ala | |
ENST00000503336.1:c.372+2120T>C | ENSP00000426053.1:n.372+2120T>C | |
NM_000112.3:c.878T>C , LRG_684t1:c.878T>C | NP_000103.2:p.Val293Ala | |
XM_017009191.2:c.878T>C | XP_016864680.1:p.Val293Ala | |
NM_000112.4:c.878T>C MANE Select | NP_000103.2:p.Val293Ala |