HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47333638G= , CM000673.2:g.47333638G= | GRCh38 |
NC_000011.9:g.47355189G= , CM000673.1:g.47355189G= | GRCh37 |
NC_000011.8:g.47311765G= | NCBI36 |
NG_007667.1:g.24065C= , LRG_386:g.24065C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.3109C= MANE Select | ENSP00000442795.1:p.Arg1037= | |
ENST00000256993.8:c.3109C= | ENSP00000256993.5:p.Arg1037= | |
ENST00000399249.6:c.3109C= | ENSP00000382193.2:p.Arg1037= | |
ENST00000545968.5:c.3109C= | ENSP00000442795.1:p.Arg1037= | |
NM_000256.3:c.3109C= , LRG_386t1:c.3109C= MANE Select | NP_000247.2:p.Arg1037= | |
XM_011520117.1:c.3091C= | XP_011518419.1:p.Arg1031= | |
XM_011520118.1:c.3028C= | XP_011518420.1:p.Arg1010= |