HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88007797_88007798insT , CM000666.2:g.88007797_88007798insT | GRCh38 |
NC_000004.11:g.88928949_88928950insT , CM000666.1:g.88928949_88928950insT | GRCh37 |
NC_000004.10:g.89147973_89147974insT | NCBI36 |
NG_008604.1:g.5130_5131insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.64_65insT MANE Select | ENSP00000237596.2:p.Arg22LeufsTer? | |
ENST00000237596.6:c.64_65insT | ENSP00000237596.2:p.Arg22LeufsTer? | |
NM_000297.3:c.64_65insT | NP_000288.1:p.Arg22LeufsTer? | |
XM_011532028.1:c.64_65insT | XP_011530330.1:p.Arg22LeufsTer? | |
XR_244632.2:n.159_160insT | ||
NR_156488.1:n.151_152insT | ||
XM_011532028.2:c.64_65insT | XP_011530330.1:p.Arg22LeufsTer? | |
NM_000297.4:c.64_65insT MANE Select | NP_000288.1:p.Arg22LeufsTer? | |
NR_156488.2:n.163_164insT |