HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32475091T>G , CM000684.2:g.32475091T>G | GRCh38 |
NC_000022.10:g.32871078T>G , CM000684.1:g.32871078T>G | GRCh37 |
NC_000022.9:g.31201078T>G | NCBI36 |
NG_016001.1:g.5372T>G | |
NG_016001.2:g.5372T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266087.12:c.89T>G MANE Select | ENSP00000266087.7:p.Leu30Arg | |
ENST00000266087.11:c.89T>G | ENSP00000266087.7:p.Leu30Arg | |
ENST00000420700.5:c.89T>G | ENSP00000406155.1:p.Leu30Arg | |
ENST00000425028.5:c.89T>G | ENSP00000395823.1:p.Leu30Arg | |
ENST00000492535.1:n.77T>G | ||
NM_012179.3:c.89T>G | NP_036311.3:p.Leu30Arg | |
XM_011530106.1:c.-85T>G | XP_011528408.1:n.-85T>G | |
XM_024452207.1:c.-102T>G | XP_024307975.1:n.-102T>G | |
NM_012179.4:c.89T>G MANE Select | NP_036311.3:p.Leu30Arg |