HGVS | Genome Assembly |
---|---|
NC_000019.10:g.1104003_1104006dup , CM000681.2:g.1104003_1104006dup | GRCh38 |
NC_000019.9:g.1104002_1104005dup , CM000681.1:g.1104002_1104005dup | GRCh37 |
NC_000019.8:g.1055002_1055005dup | NCBI36 |
NG_050621.1:g.5078_5081dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000706713.1:c.-41_-38dup | ENSP00000516510.1:n.-41_-38dup | |
ENST00000354171.13:c.-41_-38dup MANE Select | ENSP00000346103.7:n.-41_-38dup | |
ENST00000354171.12:c.-41_-38dup | ENSP00000346103.7:n.-41_-38dup | |
ENST00000616066.4:c.-41_-38dup | ENSP00000485000.1:n.-41_-38dup | |
NM_001039847.2:c.-41_-38dup | NP_001034936.1:n.-41_-38dup | |
NM_002085.4:c.-41_-38dup | NP_002076.2:n.-41_-38dup | |
NM_001039847.3:c.-41_-38dup | NP_001034936.1:n.-41_-38dup | |
NM_002085.5:c.-41_-38dup MANE Select | NP_002076.2:n.-41_-38dup |