HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154903949_154903950delinsTC , CM000685.2:g.154903949_154903950delinsTC | GRCh38 |
NC_000023.10:g.154132224_154132225delinsTC , CM000685.1:g.154132224_154132225delinsTC | GRCh37 |
NC_000023.9:g.153785418_153785419delinsTC | NCBI36 |
NG_011403.1:g.123774_123775delinsGA | |
NG_011403.2:g.123774_123775delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5954_5955delinsGA MANE Select | ENSP00000353393.4:p.Arg1985= | |
ENST00000360256.8:c.5954_5955delinsGA | ENSP00000353393.4:p.Arg1985= | |
NM_000132.3:c.5954_5955delinsGA | NP_000123.1:p.Arg1985= | |
XM_011531126.1:c.5849_5850delinsGA | XP_011529428.1:p.Arg1950= | |
NM_000132.4:c.5954_5955delinsGA MANE Select | NP_000123.1:p.Arg1985= |