HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134843165_134843168dup , CM000671.2:g.134843165_134843168dup | GRCh38 |
NC_000009.11:g.137735011_137735014dup , CM000671.1:g.137735011_137735014dup | GRCh37 |
NC_000009.10:g.136874832_136874835dup | NCBI36 |
NG_008030.1:g.206360_206363dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371820.4:c.*862_*865dup | ENSP00000360885.4:n.*862_*865dup | |
ENST00000371817.8:c.*862_*865dup MANE Select | ENSP00000360882.3:n.*862_*865dup | |
ENST00000371817.7:c.*862_*865dup | ENSP00000360882.3:n.*862_*865dup | |
ENST00000618395.4:c.*862_*865dup | ENSP00000481360.1:n.*862_*865dup | |
NM_000093.4:c.*862_*865dup | NP_000084.3:n.*862_*865dup | |
NM_001278074.1:c.*862_*865dup | NP_001265003.1:n.*862_*865dup | |
NR_103451.2:n.71-22950_71-22947dup | ||
NM_000093.5:c.*862_*865dup MANE Select | NP_000084.3:n.*862_*865dup |