HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173102_173103dup , CM000678.2:g.173102_173103dup | GRCh38 |
NC_000016.9:g.223101_223102dup , CM000678.1:g.223101_223102dup | GRCh37 |
NC_000016.8:g.163101_163102dup | NCBI36 |
NG_000006.1:g.33965_33966dup | |
NG_059186.1:g.1452_1453dup | |
NG_059271.1:g.5256_5257dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251595.11:c.96-23_96-22dup MANE Select | ENSP00000251595.6:n.96-23_96-22dup | |
ENST00000251595.10:c.96-23_96-22dup | ENSP00000251595.6:n.96-23_96-22dup | |
ENST00000397806.1:c.-1-23_-1-22dup | ENSP00000380908.1:n.-1-23_-1-22dup | |
ENST00000482565.1:n.209_210dup | ||
ENST00000484216.1:n.65-23_65-22dup | ||
NM_000517.4:c.96-23_96-22dup | NP_000508.1:n.96-23_96-22dup | |
NM_000517.6:c.96-23_96-22dup MANE Select | NP_000508.1:n.96-23_96-22dup |